Name: rs34670843
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs34670843

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:19052415-19052440 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(CA)₅ / del(CA)₄ / del(CA)₃ / d…
del(CA)₅ / del(CA)₄ / del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄ / dup(CA)₅ / dup(CA)₆ / dup(CA)₇ / dup(CA)₈ / dup(CA)₉ / dup(CA)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupCACA=0.1147 (822/7166, ALFA)
dupCACA=0.3355 (1680/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DGCR2 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	7166	CACACACACACACACACACACACACA=0.7014	CACACACACACACACA=0.0000, CACACACACACACACACA=0.0000, CACACACACACACACACACA=0.0000, CACACACACACACACACACACA=0.0000, CACACACACACACACACACACACA=0.0112, CACACACACACACACACACACACACACA=0.0666, CACACACACACACACACACACACACACACACA=0.0878, CACACACACACACACACACACACACACACA=0.1147, CACACACACACACACACACACACACACACACACA=0.0177, CACACACACACACACACACACACACACACACACACA=0.0007, CACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACACACACA=0.0000	0.796617	0.036246	0.167137	32
European	Sub	6460	CACACACACACACACACACACACACA=0.6693	CACACACACACACACA=0.0000, CACACACACACACACACA=0.0000, CACACACACACACACACACA=0.0000, CACACACACACACACACACACA=0.0000, CACACACACACACACACACACACA=0.0124, CACACACACACACACACACACACACACA=0.0737, CACACACACACACACACACACACACACACACA=0.0969, CACACACACACACACACACACACACACACA=0.1272, CACACACACACACACACACACACACACACACACA=0.0197, CACACACACACACACACACACACACACACACACACA=0.0008, CACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACACACACACACACACA=0.0000	0.763244	0.042194	0.194562	32
African	Sub	400	CACACACACACACACACACACACACA=1.000	CACACACACACACACA=0.000, CACACACACACACACACA=0.000, CACACACACACACACACACA=0.000, CACACACACACACACACACACA=0.000, CACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	CACACACACACACACACACACACACA=1.00	CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	388	CACACACACACACACACACACACACA=1.000	CACACACACACACACA=0.000, CACACACACACACACACA=0.000, CACACACACACACACACACA=0.000, CACACACACACACACACACACA=0.000, CACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	CACACACACACACACACACACACACA=1.00	CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	20	CACACACACACACACACACACACACA=1.00	CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	CACACACACACACACACACACACACA=1.0	CACACACACACACACA=0.0, CACACACACACACACACA=0.0, CACACACACACACACACACA=0.0, CACACACACACACACACACACA=0.0, CACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACACACACACACA=0.0, CACACACACACACACACACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	30	CACACACACACACACACACACACACA=1.00	CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	158	CACACACACACACACACACACACACA=1.000	CACACACACACACACA=0.000, CACACACACACACACACA=0.000, CACACACACACACACACACA=0.000, CACACACACACACACACACACA=0.000, CACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	14	CACACACACACACACACACACACACA=1.00	CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other	Sub	78	CACACACACACACACACACACACACA=0.95	CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.01, CACACACACACACACACACACACACACACACA=0.04, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7166	(CA)₁₃=0.7014	del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0112, dupCA=0.0666, dupCACA=0.1147, dup(CA)₃=0.0878, dup(CA)₄=0.0177, dup(CA)₅=0.0007, dup(CA)₆=0.0000, dup(CA)₇=0.0000, dup(CA)₈=0.0000, dup(CA)₉=0.0000, dup(CA)₁₀=0.0000
Allele Frequency Aggregator	European	Sub	6460	(CA)₁₃=0.6693	del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0124, dupCA=0.0737, dupCACA=0.1272, dup(CA)₃=0.0969, dup(CA)₄=0.0197, dup(CA)₅=0.0008, dup(CA)₆=0.0000, dup(CA)₇=0.0000, dup(CA)₈=0.0000, dup(CA)₉=0.0000, dup(CA)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	400	(CA)₁₃=1.000	del(CA)₅=0.000, del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000, dup(CA)₈=0.000, dup(CA)₉=0.000, dup(CA)₁₀=0.000
Allele Frequency Aggregator	Latin American 2	Sub	158	(CA)₁₃=1.000	del(CA)₅=0.000, del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000, dup(CA)₈=0.000, dup(CA)₉=0.000, dup(CA)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	78	(CA)₁₃=0.95	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.01, dupCACA=0.00, dup(CA)₃=0.04, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00, dup(CA)₉=0.00, dup(CA)₁₀=0.00
Allele Frequency Aggregator	Latin American 1	Sub	30	(CA)₁₃=1.00	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00, dup(CA)₉=0.00, dup(CA)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	26	(CA)₁₃=1.00	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00, dup(CA)₉=0.00, dup(CA)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(CA)₁₃=1.00	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00, dup(CA)₈=0.00, dup(CA)₉=0.00, dup(CA)₁₀=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCACA=0.3355
1000Genomes	African	Sub	1322	- No frequency provided	dupCACA=0.5121
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCACA=0.2738
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCACA=0.2008
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCACA=0.372
1000Genomes	American	Sub	694	- No frequency provided	dupCACA=0.232

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[8]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[9]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[10]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[11]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[12]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[14]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[15]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[16]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[17]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[18]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[19]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[20]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[21]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[22]
GRCh38.p14 chr 22	NC_000022.11:g.19052415CA[23]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[8]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[9]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[10]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[11]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[12]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[14]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[15]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[16]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[17]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[18]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[19]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[20]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[21]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[22]
GRCh37.p13 chr 22	NC_000022.10:g.19039928CA[23]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[8]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[9]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[10]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[11]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[12]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[14]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[15]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[16]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[17]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[18]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[19]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[20]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[21]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[22]
DGCR2 RefSeqGene	NG_021333.2:g.75015TG[23]

Gene: DGCR2, DiGeorge syndrome critical region gene 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DGCR2 transcript variant 2	NM_001173533.2:c.680-3797… NM_001173533.2:c.680-3797TG[8]	N/A	Intron Variant
DGCR2 transcript variant 3	NM_001173534.2:c.671-3797… NM_001173534.2:c.671-3797TG[8]	N/A	Intron Variant
DGCR2 transcript variant 4	NM_001184781.2:c.794-3797… NM_001184781.2:c.794-3797TG[8]	N/A	Intron Variant
DGCR2 transcript variant 1	NM_005137.3:c.803-3797TG[… NM_005137.3:c.803-3797TG[8]	N/A	Intron Variant
DGCR2 transcript variant 5	NR_033674.2:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(CA)₁₃=	del(CA)₅	del(CA)₄	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄	dup(CA)₅	dup(CA)₆	dup(CA)₇	dup(CA)₈	dup(CA)₉	dup(CA)₁₀
GRCh38.p14 chr 22	NC_000022.11:g.19052415_19052440=	NC_000022.11:g.19052415CA[8]	NC_000022.11:g.19052415CA[9]	NC_000022.11:g.19052415CA[10]	NC_000022.11:g.19052415CA[11]	NC_000022.11:g.19052415CA[12]	NC_000022.11:g.19052415CA[14]	NC_000022.11:g.19052415CA[15]	NC_000022.11:g.19052415CA[16]	NC_000022.11:g.19052415CA[17]	NC_000022.11:g.19052415CA[18]	NC_000022.11:g.19052415CA[19]	NC_000022.11:g.19052415CA[20]	NC_000022.11:g.19052415CA[21]	NC_000022.11:g.19052415CA[22]	NC_000022.11:g.19052415CA[23]
GRCh37.p13 chr 22	NC_000022.10:g.19039928_19039953=	NC_000022.10:g.19039928CA[8]	NC_000022.10:g.19039928CA[9]	NC_000022.10:g.19039928CA[10]	NC_000022.10:g.19039928CA[11]	NC_000022.10:g.19039928CA[12]	NC_000022.10:g.19039928CA[14]	NC_000022.10:g.19039928CA[15]	NC_000022.10:g.19039928CA[16]	NC_000022.10:g.19039928CA[17]	NC_000022.10:g.19039928CA[18]	NC_000022.10:g.19039928CA[19]	NC_000022.10:g.19039928CA[20]	NC_000022.10:g.19039928CA[21]	NC_000022.10:g.19039928CA[22]	NC_000022.10:g.19039928CA[23]
DGCR2 RefSeqGene	NG_021333.2:g.75015_75040=	NG_021333.2:g.75015TG[8]	NG_021333.2:g.75015TG[9]	NG_021333.2:g.75015TG[10]	NG_021333.2:g.75015TG[11]	NG_021333.2:g.75015TG[12]	NG_021333.2:g.75015TG[14]	NG_021333.2:g.75015TG[15]	NG_021333.2:g.75015TG[16]	NG_021333.2:g.75015TG[17]	NG_021333.2:g.75015TG[18]	NG_021333.2:g.75015TG[19]	NG_021333.2:g.75015TG[20]	NG_021333.2:g.75015TG[21]	NG_021333.2:g.75015TG[22]	NG_021333.2:g.75015TG[23]
DGCR2 transcript variant 2	NM_001173533.1:c.680-3772=	NM_001173533.1:c.680-3797TG[8]	NM_001173533.1:c.680-3797TG[9]	NM_001173533.1:c.680-3797TG[10]	NM_001173533.1:c.680-3797TG[11]	NM_001173533.1:c.680-3797TG[12]	NM_001173533.1:c.680-3797TG[14]	NM_001173533.1:c.680-3797TG[15]	NM_001173533.1:c.680-3797TG[16]	NM_001173533.1:c.680-3797TG[17]	NM_001173533.1:c.680-3797TG[18]	NM_001173533.1:c.680-3797TG[19]	NM_001173533.1:c.680-3797TG[20]	NM_001173533.1:c.680-3797TG[21]	NM_001173533.1:c.680-3797TG[22]	NM_001173533.1:c.680-3797TG[23]
DGCR2 transcript variant 2	NM_001173533.2:c.680-3772=	NM_001173533.2:c.680-3797TG[8]	NM_001173533.2:c.680-3797TG[9]	NM_001173533.2:c.680-3797TG[10]	NM_001173533.2:c.680-3797TG[11]	NM_001173533.2:c.680-3797TG[12]	NM_001173533.2:c.680-3797TG[14]	NM_001173533.2:c.680-3797TG[15]	NM_001173533.2:c.680-3797TG[16]	NM_001173533.2:c.680-3797TG[17]	NM_001173533.2:c.680-3797TG[18]	NM_001173533.2:c.680-3797TG[19]	NM_001173533.2:c.680-3797TG[20]	NM_001173533.2:c.680-3797TG[21]	NM_001173533.2:c.680-3797TG[22]	NM_001173533.2:c.680-3797TG[23]
DGCR2 transcript variant 3	NM_001173534.1:c.671-3772=	NM_001173534.1:c.671-3797TG[8]	NM_001173534.1:c.671-3797TG[9]	NM_001173534.1:c.671-3797TG[10]	NM_001173534.1:c.671-3797TG[11]	NM_001173534.1:c.671-3797TG[12]	NM_001173534.1:c.671-3797TG[14]	NM_001173534.1:c.671-3797TG[15]	NM_001173534.1:c.671-3797TG[16]	NM_001173534.1:c.671-3797TG[17]	NM_001173534.1:c.671-3797TG[18]	NM_001173534.1:c.671-3797TG[19]	NM_001173534.1:c.671-3797TG[20]	NM_001173534.1:c.671-3797TG[21]	NM_001173534.1:c.671-3797TG[22]	NM_001173534.1:c.671-3797TG[23]
DGCR2 transcript variant 3	NM_001173534.2:c.671-3772=	NM_001173534.2:c.671-3797TG[8]	NM_001173534.2:c.671-3797TG[9]	NM_001173534.2:c.671-3797TG[10]	NM_001173534.2:c.671-3797TG[11]	NM_001173534.2:c.671-3797TG[12]	NM_001173534.2:c.671-3797TG[14]	NM_001173534.2:c.671-3797TG[15]	NM_001173534.2:c.671-3797TG[16]	NM_001173534.2:c.671-3797TG[17]	NM_001173534.2:c.671-3797TG[18]	NM_001173534.2:c.671-3797TG[19]	NM_001173534.2:c.671-3797TG[20]	NM_001173534.2:c.671-3797TG[21]	NM_001173534.2:c.671-3797TG[22]	NM_001173534.2:c.671-3797TG[23]
DGCR2 transcript variant 4	NM_001184781.1:c.794-3772=	NM_001184781.1:c.794-3797TG[8]	NM_001184781.1:c.794-3797TG[9]	NM_001184781.1:c.794-3797TG[10]	NM_001184781.1:c.794-3797TG[11]	NM_001184781.1:c.794-3797TG[12]	NM_001184781.1:c.794-3797TG[14]	NM_001184781.1:c.794-3797TG[15]	NM_001184781.1:c.794-3797TG[16]	NM_001184781.1:c.794-3797TG[17]	NM_001184781.1:c.794-3797TG[18]	NM_001184781.1:c.794-3797TG[19]	NM_001184781.1:c.794-3797TG[20]	NM_001184781.1:c.794-3797TG[21]	NM_001184781.1:c.794-3797TG[22]	NM_001184781.1:c.794-3797TG[23]
DGCR2 transcript variant 4	NM_001184781.2:c.794-3772=	NM_001184781.2:c.794-3797TG[8]	NM_001184781.2:c.794-3797TG[9]	NM_001184781.2:c.794-3797TG[10]	NM_001184781.2:c.794-3797TG[11]	NM_001184781.2:c.794-3797TG[12]	NM_001184781.2:c.794-3797TG[14]	NM_001184781.2:c.794-3797TG[15]	NM_001184781.2:c.794-3797TG[16]	NM_001184781.2:c.794-3797TG[17]	NM_001184781.2:c.794-3797TG[18]	NM_001184781.2:c.794-3797TG[19]	NM_001184781.2:c.794-3797TG[20]	NM_001184781.2:c.794-3797TG[21]	NM_001184781.2:c.794-3797TG[22]	NM_001184781.2:c.794-3797TG[23]
DGCR2 transcript variant 1	NM_005137.2:c.803-3772=	NM_005137.2:c.803-3797TG[8]	NM_005137.2:c.803-3797TG[9]	NM_005137.2:c.803-3797TG[10]	NM_005137.2:c.803-3797TG[11]	NM_005137.2:c.803-3797TG[12]	NM_005137.2:c.803-3797TG[14]	NM_005137.2:c.803-3797TG[15]	NM_005137.2:c.803-3797TG[16]	NM_005137.2:c.803-3797TG[17]	NM_005137.2:c.803-3797TG[18]	NM_005137.2:c.803-3797TG[19]	NM_005137.2:c.803-3797TG[20]	NM_005137.2:c.803-3797TG[21]	NM_005137.2:c.803-3797TG[22]	NM_005137.2:c.803-3797TG[23]
DGCR2 transcript variant 1	NM_005137.3:c.803-3772=	NM_005137.3:c.803-3797TG[8]	NM_005137.3:c.803-3797TG[9]	NM_005137.3:c.803-3797TG[10]	NM_005137.3:c.803-3797TG[11]	NM_005137.3:c.803-3797TG[12]	NM_005137.3:c.803-3797TG[14]	NM_005137.3:c.803-3797TG[15]	NM_005137.3:c.803-3797TG[16]	NM_005137.3:c.803-3797TG[17]	NM_005137.3:c.803-3797TG[18]	NM_005137.3:c.803-3797TG[19]	NM_005137.3:c.803-3797TG[20]	NM_005137.3:c.803-3797TG[21]	NM_005137.3:c.803-3797TG[22]	NM_005137.3:c.803-3797TG[23]

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

82 SubSNP, 45 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41508577	Mar 14, 2006 (126)
2	HGSV	ss81832398	Oct 12, 2018 (152)
3	HGSV	ss82059572	Oct 12, 2018 (152)
4	HUMANGENOME_JCVI	ss95753988	Oct 12, 2018 (152)
5	BUSHMAN	ss193639860	Jul 04, 2010 (132)
6	1000GENOMES	ss327997261	May 09, 2011 (134)
7	1000GENOMES	ss328099451	May 09, 2011 (134)
8	1000GENOMES	ss328321655	May 09, 2011 (134)
9	LUNTER	ss552707906	Apr 25, 2013 (138)
10	LUNTER	ss553130324	Apr 25, 2013 (138)
11	LUNTER	ss553699016	Apr 25, 2013 (138)
12	SSMP	ss664515859	Apr 01, 2015 (144)
13	1000GENOMES	ss1378891812	Aug 21, 2014 (142)
14	DDI	ss1536926515	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1709539398	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1709539400	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1709539401	Oct 12, 2018 (152)
18	EVA_UK10K_TWINSUK	ss1709539531	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1709539534	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1709539537	Oct 12, 2018 (152)
21	HAMMER_LAB	ss1809730751	Sep 08, 2015 (146)
22	HAMMER_LAB	ss1809730752	Sep 08, 2015 (146)
23	SWEGEN	ss3019074165	Jan 10, 2018 (151)
24	MCHAISSO	ss3065848918	Nov 08, 2017 (151)
25	URBANLAB	ss3651150602	Oct 12, 2018 (152)
26	ACPOP	ss3743816747	Jul 13, 2019 (153)
27	ACPOP	ss3743816748	Jul 13, 2019 (153)
28	ACPOP	ss3743816749	Jul 13, 2019 (153)
29	ACPOP	ss3743816750	Jul 13, 2019 (153)
30	PACBIO	ss3788791359	Jul 13, 2019 (153)
31	PACBIO	ss3793662745	Jul 13, 2019 (153)
32	PACBIO	ss3798549064	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3822390132	Jul 13, 2019 (153)
34	EVA	ss3835923841	Apr 27, 2020 (154)
35	KOGIC	ss3983373813	Apr 27, 2020 (154)
36	KOGIC	ss3983373814	Apr 27, 2020 (154)
37	KOGIC	ss3983373815	Apr 27, 2020 (154)
38	KOGIC	ss3983373816	Apr 27, 2020 (154)
39	KOGIC	ss3983373817	Apr 27, 2020 (154)
40	KOGIC	ss3983373818	Apr 27, 2020 (154)
41	GNOMAD	ss4362433167	Apr 27, 2021 (155)
42	GNOMAD	ss4362433168	Apr 27, 2021 (155)
43	GNOMAD	ss4362433169	Apr 27, 2021 (155)
44	GNOMAD	ss4362433170	Apr 27, 2021 (155)
45	GNOMAD	ss4362433171	Apr 27, 2021 (155)
46	GNOMAD	ss4362433172	Apr 27, 2021 (155)
47	GNOMAD	ss4362433173	Apr 27, 2021 (155)
48	GNOMAD	ss4362433174	Apr 27, 2021 (155)
49	GNOMAD	ss4362433175	Apr 27, 2021 (155)
50	GNOMAD	ss4362433176	Apr 27, 2021 (155)
51	GNOMAD	ss4362433178	Apr 27, 2021 (155)
52	GNOMAD	ss4362433179	Apr 27, 2021 (155)
53	GNOMAD	ss4362433180	Apr 27, 2021 (155)
54	GNOMAD	ss4362433181	Apr 27, 2021 (155)
55	GNOMAD	ss4362433182	Apr 27, 2021 (155)
56	TOMMO_GENOMICS	ss5232007810	Apr 27, 2021 (155)
57	TOMMO_GENOMICS	ss5232007811	Apr 27, 2021 (155)
58	TOMMO_GENOMICS	ss5232007812	Apr 27, 2021 (155)
59	TOMMO_GENOMICS	ss5232007813	Apr 27, 2021 (155)
60	TOMMO_GENOMICS	ss5232007814	Apr 27, 2021 (155)
61	TOMMO_GENOMICS	ss5232007815	Apr 27, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5310633308	Oct 16, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5310633309	Oct 16, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5310633310	Oct 16, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5310633311	Oct 16, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5310633312	Oct 16, 2022 (156)
67	HUGCELL_USP	ss5502546910	Oct 16, 2022 (156)
68	HUGCELL_USP	ss5502546911	Oct 16, 2022 (156)
69	HUGCELL_USP	ss5502546912	Oct 16, 2022 (156)
70	HUGCELL_USP	ss5502546913	Oct 16, 2022 (156)
71	HUGCELL_USP	ss5502546914	Oct 16, 2022 (156)
72	HUGCELL_USP	ss5502546915	Oct 16, 2022 (156)
73	TOMMO_GENOMICS	ss5792948118	Oct 16, 2022 (156)
74	TOMMO_GENOMICS	ss5792948119	Oct 16, 2022 (156)
75	TOMMO_GENOMICS	ss5792948120	Oct 16, 2022 (156)
76	TOMMO_GENOMICS	ss5792948121	Oct 16, 2022 (156)
77	TOMMO_GENOMICS	ss5792948122	Oct 16, 2022 (156)
78	TOMMO_GENOMICS	ss5792948123	Oct 16, 2022 (156)
79	EVA	ss5821889979	Oct 16, 2022 (156)
80	EVA	ss5821889980	Oct 16, 2022 (156)
81	EVA	ss5881320151	Oct 16, 2022 (156)
82	EVA	ss5981123192	Oct 16, 2022 (156)
83	1000Genomes	NC_000022.10 - 19039928	Oct 12, 2018 (152)
84	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 44365722 (NC_000022.10:19039927::CA 501/3854) Row 44365723 (NC_000022.10:19039927::CACA 1036/3854) Row 44365724 (NC_000022.10:19039953::CA 514/3854)	-	Oct 12, 2018 (152)
85	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 44365722 (NC_000022.10:19039927::CA 501/3854) Row 44365723 (NC_000022.10:19039927::CACA 1036/3854) Row 44365724 (NC_000022.10:19039953::CA 514/3854)	-	Oct 12, 2018 (152)
86	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 44365722 (NC_000022.10:19039927::CA 501/3854) Row 44365723 (NC_000022.10:19039927::CACA 1036/3854) Row 44365724 (NC_000022.10:19039953::CA 514/3854)	-	Oct 12, 2018 (152)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566346199 (NC_000022.11:19052414::CA 11284/136666) Row 566346200 (NC_000022.11:19052414::CACA 34734/136576) Row 566346201 (NC_000022.11:19052414::CACACA 14881/136664)...	-	Apr 27, 2021 (155)
102	Korean Genome Project Submission ignored due to conflicting rows: Row 39751814 (NC_000022.11:19052422::CA 162/1832) Row 39751815 (NC_000022.11:19052422::CACA 518/1832) Row 39751816 (NC_000022.11:19052422::CACACA 203/1832)...	-	Apr 27, 2020 (154)
103	Korean Genome Project Submission ignored due to conflicting rows: Row 39751814 (NC_000022.11:19052422::CA 162/1832) Row 39751815 (NC_000022.11:19052422::CACA 518/1832) Row 39751816 (NC_000022.11:19052422::CACACA 203/1832)...	-	Apr 27, 2020 (154)
104	Korean Genome Project Submission ignored due to conflicting rows: Row 39751814 (NC_000022.11:19052422::CA 162/1832) Row 39751815 (NC_000022.11:19052422::CACA 518/1832) Row 39751816 (NC_000022.11:19052422::CACACA 203/1832)...	-	Apr 27, 2020 (154)
105	Korean Genome Project Submission ignored due to conflicting rows: Row 39751814 (NC_000022.11:19052422::CA 162/1832) Row 39751815 (NC_000022.11:19052422::CACA 518/1832) Row 39751816 (NC_000022.11:19052422::CACACA 203/1832)...	-	Apr 27, 2020 (154)
106	Korean Genome Project Submission ignored due to conflicting rows: Row 39751814 (NC_000022.11:19052422::CA 162/1832) Row 39751815 (NC_000022.11:19052422::CACA 518/1832) Row 39751816 (NC_000022.11:19052422::CACACA 203/1832)...	-	Apr 27, 2020 (154)
107	Korean Genome Project Submission ignored due to conflicting rows: Row 39751814 (NC_000022.11:19052422::CA 162/1832) Row 39751815 (NC_000022.11:19052422::CACA 518/1832) Row 39751816 (NC_000022.11:19052422::CACACA 203/1832)...	-	Apr 27, 2020 (154)
108	Northern Sweden Submission ignored due to conflicting rows: Row 17101612 (NC_000022.10:19039927::CACA 130/600) Row 17101613 (NC_000022.10:19039927::CACACACA 38/600) Row 17101614 (NC_000022.10:19039927::CACACA 76/600)...	-	Jul 13, 2019 (153)
109	Northern Sweden Submission ignored due to conflicting rows: Row 17101612 (NC_000022.10:19039927::CACA 130/600) Row 17101613 (NC_000022.10:19039927::CACACACA 38/600) Row 17101614 (NC_000022.10:19039927::CACACA 76/600)...	-	Jul 13, 2019 (153)
110	Northern Sweden Submission ignored due to conflicting rows: Row 17101612 (NC_000022.10:19039927::CACA 130/600) Row 17101613 (NC_000022.10:19039927::CACACACA 38/600) Row 17101614 (NC_000022.10:19039927::CACACA 76/600)...	-	Jul 13, 2019 (153)
111	Northern Sweden Submission ignored due to conflicting rows: Row 17101612 (NC_000022.10:19039927::CACA 130/600) Row 17101613 (NC_000022.10:19039927::CACACACA 38/600) Row 17101614 (NC_000022.10:19039927::CACACA 76/600)...	-	Jul 13, 2019 (153)
112	8.3KJPN Submission ignored due to conflicting rows: Row 89977117 (NC_000022.10:19039927::CACACA 2193/16758) Row 89977118 (NC_000022.10:19039927::CACA 3963/16758) Row 89977119 (NC_000022.10:19039927::CA 1101/16758)...	-	Apr 27, 2021 (155)
113	8.3KJPN Submission ignored due to conflicting rows: Row 89977117 (NC_000022.10:19039927::CACACA 2193/16758) Row 89977118 (NC_000022.10:19039927::CACA 3963/16758) Row 89977119 (NC_000022.10:19039927::CA 1101/16758)...	-	Apr 27, 2021 (155)
114	8.3KJPN Submission ignored due to conflicting rows: Row 89977117 (NC_000022.10:19039927::CACACA 2193/16758) Row 89977118 (NC_000022.10:19039927::CACA 3963/16758) Row 89977119 (NC_000022.10:19039927::CA 1101/16758)...	-	Apr 27, 2021 (155)
115	8.3KJPN Submission ignored due to conflicting rows: Row 89977117 (NC_000022.10:19039927::CACACA 2193/16758) Row 89977118 (NC_000022.10:19039927::CACA 3963/16758) Row 89977119 (NC_000022.10:19039927::CA 1101/16758)...	-	Apr 27, 2021 (155)
116	8.3KJPN Submission ignored due to conflicting rows: Row 89977117 (NC_000022.10:19039927::CACACA 2193/16758) Row 89977118 (NC_000022.10:19039927::CACA 3963/16758) Row 89977119 (NC_000022.10:19039927::CA 1101/16758)...	-	Apr 27, 2021 (155)
117	8.3KJPN Submission ignored due to conflicting rows: Row 89977117 (NC_000022.10:19039927::CACACA 2193/16758) Row 89977118 (NC_000022.10:19039927::CACA 3963/16758) Row 89977119 (NC_000022.10:19039927::CA 1101/16758)...	-	Apr 27, 2021 (155)
118	14KJPN Submission ignored due to conflicting rows: Row 126785222 (NC_000022.11:19052414::CACA 6384/28168) Row 126785223 (NC_000022.11:19052414::CACACA 3376/28168) Row 126785224 (NC_000022.11:19052414::CA 1695/28168)...	-	Oct 16, 2022 (156)
119	14KJPN Submission ignored due to conflicting rows: Row 126785222 (NC_000022.11:19052414::CACA 6384/28168) Row 126785223 (NC_000022.11:19052414::CACACA 3376/28168) Row 126785224 (NC_000022.11:19052414::CA 1695/28168)...	-	Oct 16, 2022 (156)
120	14KJPN Submission ignored due to conflicting rows: Row 126785222 (NC_000022.11:19052414::CACA 6384/28168) Row 126785223 (NC_000022.11:19052414::CACACA 3376/28168) Row 126785224 (NC_000022.11:19052414::CA 1695/28168)...	-	Oct 16, 2022 (156)
121	14KJPN Submission ignored due to conflicting rows: Row 126785222 (NC_000022.11:19052414::CACA 6384/28168) Row 126785223 (NC_000022.11:19052414::CACACA 3376/28168) Row 126785224 (NC_000022.11:19052414::CA 1695/28168)...	-	Oct 16, 2022 (156)
122	14KJPN Submission ignored due to conflicting rows: Row 126785222 (NC_000022.11:19052414::CACA 6384/28168) Row 126785223 (NC_000022.11:19052414::CACACA 3376/28168) Row 126785224 (NC_000022.11:19052414::CA 1695/28168)...	-	Oct 16, 2022 (156)
123	14KJPN Submission ignored due to conflicting rows: Row 126785222 (NC_000022.11:19052414::CACA 6384/28168) Row 126785223 (NC_000022.11:19052414::CACACA 3376/28168) Row 126785224 (NC_000022.11:19052414::CA 1695/28168)...	-	Oct 16, 2022 (156)
124	UK 10K study - Twins Submission ignored due to conflicting rows: Row 44365722 (NC_000022.10:19039927::CA 421/3708) Row 44365723 (NC_000022.10:19039927::CACA 970/3708) Row 44365724 (NC_000022.10:19039953::CA 435/3708)	-	Oct 12, 2018 (152)
125	UK 10K study - Twins Submission ignored due to conflicting rows: Row 44365722 (NC_000022.10:19039927::CA 421/3708) Row 44365723 (NC_000022.10:19039927::CACA 970/3708) Row 44365724 (NC_000022.10:19039953::CA 435/3708)	-	Oct 12, 2018 (152)
126	UK 10K study - Twins Submission ignored due to conflicting rows: Row 44365722 (NC_000022.10:19039927::CA 421/3708) Row 44365723 (NC_000022.10:19039927::CACA 970/3708) Row 44365724 (NC_000022.10:19039953::CA 435/3708)	-	Oct 12, 2018 (152)
127	ALFA	NC_000022.11 - 19052415	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4362433182	NC_000022.11:19052414:CACACACACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACA	(self)
ss3983373818, ss4362433181	NC_000022.11:19052414:CACACACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACA	(self)
ss1536926515, ss1809730752	NC_000022.10:19039927:CACACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACA	(self)
ss4362433180, ss5310633308, ss5502546914, ss5881320151	NC_000022.11:19052414:CACACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACA	(self)
ss5232007814	NC_000022.10:19039927:CACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
ss4362433179, ss5792948122	NC_000022.11:19052414:CACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
ss193639860	NT_011520.13:342850:CACA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
ss3019074165, ss3788791359, ss3793662745, ss3798549064	NC_000022.10:19039927:CA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACA	(self)
ss4362433178, ss5502546911	NC_000022.11:19052414:CA:	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACA	(self)
ss1709539398, ss1709539531, ss3743816750, ss5232007812, ss5821889979, ss5981123192	NC_000022.10:19039927::CA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss1709539401, ss1709539537	NC_000022.10:19039953::CA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss4362433167, ss5310633309, ss5502546915, ss5792948120	NC_000022.11:19052414::CA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss3983373813	NC_000022.11:19052422::CA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss3651150602	NC_000022.11:19052437::AC	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss41508577	NT_011519.10:2192102::AC	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss95753988	NT_011519.10:2192103::CA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss327997261, ss328099451, ss328321655, ss552707906, ss553130324	NC_000022.9:17419927::CACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
80188455, ss664515859, ss1378891812, ss1709539400, ss1709539534, ss3743816747, ss3835923841, ss5232007811, ss5821889980	NC_000022.10:19039927::CACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
ss3065848918, ss3822390132, ss4362433168, ss5310633311, ss5502546910, ss5792948118	NC_000022.11:19052414::CACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
ss3983373814	NC_000022.11:19052422::CACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
ss553699016	NC_000022.9:17419927::CACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)
ss1809730751, ss3743816749, ss5232007810	NC_000022.10:19039927::CACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)
ss4362433169, ss5310633310, ss5502546912, ss5792948119	NC_000022.11:19052414::CACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)
ss3983373815	NC_000022.11:19052422::CACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)
ss81832398, ss82059572	NT_011519.10:2192103::CACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)
ss3743816748, ss5232007813	NC_000022.10:19039927::CACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA	(self)
ss4362433170, ss5310633312, ss5502546913, ss5792948121	NC_000022.11:19052414::CACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA	(self)
ss3983373816	NC_000022.11:19052422::CACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA	(self)
ss5232007815	NC_000022.10:19039927::CACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA	(self)
ss4362433171, ss5792948123	NC_000022.11:19052414::CACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA	(self)
ss3983373817	NC_000022.11:19052422::CACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA	(self)
ss4362433172	NC_000022.11:19052414::CACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA	(self)
ss4362433173	NC_000022.11:19052414::CACACACACAC… NC_000022.11:19052414::CACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA	(self)
ss4362433174	NC_000022.11:19052414::CACACACACAC… NC_000022.11:19052414::CACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA	(self)
ss4362433175	NC_000022.11:19052414::CACACACACAC… NC_000022.11:19052414::CACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA	(self)
ss4362433176	NC_000022.11:19052414::CACACACACAC… NC_000022.11:19052414::CACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA	(self)
17039329662	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA	NC_000022.11:19052414:CACACACACACA… NC_000022.11:19052414:CACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34670843

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34670843