Name: rs11370226
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.

rs11370226

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:62948804-62948822 (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(T)₁₀ / del(T)₉ / del(T)₈ / del…
del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / insTTTC(T)₄AATTTAC(T)₂₃ / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / ins(T)₃₅
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.2237 (1456/6509, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GID8 : 500B Downstream 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	HWEP
Total	Global	2174	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	1318	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	574	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	20	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	554	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	28	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	24	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	N/A
Latin American 1	Sub	38	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	114	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	14	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	88	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6509	(T)₁₉=0.7334	del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0241, dupT=0.0101, dupTT=0.2237, dupTTT=0.0037, dup(T)₄=0.0049
Allele Frequency Aggregator	European	Sub	5645	(T)₁₉=0.6935	del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0278, dupT=0.0117, dupTT=0.2572, dupTTT=0.0043, dup(T)₄=0.0055
Allele Frequency Aggregator	African	Sub	574	(T)₁₉=1.000	del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	114	(T)₁₉=1.000	del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	96	(T)₁₉=0.95	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.04, dupTTT=0.00, dup(T)₄=0.01
Allele Frequency Aggregator	Latin American 1	Sub	38	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	28	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00

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 20	NC_000020.11:g.62948813_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948814_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948815_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948817_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948818_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948819_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948820_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948821_62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948822del
GRCh38.p14 chr 20	NC_000020.11:g.62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948821_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948820_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948804_62948822T[22]CTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 20	NC_000020.11:g.62948819_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948818_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948817_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948816_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948815_62948822dup
GRCh38.p14 chr 20	NC_000020.11:g.62948822_62948823insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20	NC_000020.10:g.61580165_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580166_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580167_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580169_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580170_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580171_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580172_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580173_61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580174del
GRCh37.p13 chr 20	NC_000020.10:g.61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580173_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580172_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580156_61580174T[22]CTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 20	NC_000020.10:g.61580171_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580170_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580169_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580168_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580167_61580174dup
GRCh37.p13 chr 20	NC_000020.10:g.61580174_61580175insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC17A9 RefSeqGene	NG_041785.1:g.1167_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1168_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1169_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1171_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1172_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1173_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1174_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1175_1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1176del
SLC17A9 RefSeqGene	NG_041785.1:g.1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1175_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1174_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1158_1176T[22]CTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT[1]
SLC17A9 RefSeqGene	NG_041785.1:g.1173_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1172_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1171_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1170_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1169_1176dup
SLC17A9 RefSeqGene	NG_041785.1:g.1176_1177insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: GID8, GID complex subunit 8 homolog (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
GID8 transcript	NM_017896.3:c.	N/A	Downstream Transcript Variant
GID8 transcript variant X1	XM_047440246.1:c.	N/A	Downstream Transcript Variant
GID8 transcript variant X2	XM_047440247.1:c.	N/A	Downstream Transcript 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	(T)₁₉=	del(T)₁₀	del(T)₉	del(T)₈	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	insTTTC(T)₄AATTTAC(T)₂₃	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	ins(T)₃₅
GRCh38.p14 chr 20	NC_000020.11:g.62948804_62948822=	NC_000020.11:g.62948813_62948822del	NC_000020.11:g.62948814_62948822del	NC_000020.11:g.62948815_62948822del	NC_000020.11:g.62948817_62948822del	NC_000020.11:g.62948818_62948822del	NC_000020.11:g.62948819_62948822del	NC_000020.11:g.62948820_62948822del	NC_000020.11:g.62948821_62948822del	NC_000020.11:g.62948822del	NC_000020.11:g.62948822dup	NC_000020.11:g.62948821_62948822dup	NC_000020.11:g.62948820_62948822dup	NC_000020.11:g.62948804_62948822T[22]CTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000020.11:g.62948819_62948822dup	NC_000020.11:g.62948818_62948822dup	NC_000020.11:g.62948817_62948822dup	NC_000020.11:g.62948816_62948822dup	NC_000020.11:g.62948815_62948822dup	NC_000020.11:g.62948822_62948823insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 20	NC_000020.10:g.61580156_61580174=	NC_000020.10:g.61580165_61580174del	NC_000020.10:g.61580166_61580174del	NC_000020.10:g.61580167_61580174del	NC_000020.10:g.61580169_61580174del	NC_000020.10:g.61580170_61580174del	NC_000020.10:g.61580171_61580174del	NC_000020.10:g.61580172_61580174del	NC_000020.10:g.61580173_61580174del	NC_000020.10:g.61580174del	NC_000020.10:g.61580174dup	NC_000020.10:g.61580173_61580174dup	NC_000020.10:g.61580172_61580174dup	NC_000020.10:g.61580156_61580174T[22]CTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000020.10:g.61580171_61580174dup	NC_000020.10:g.61580170_61580174dup	NC_000020.10:g.61580169_61580174dup	NC_000020.10:g.61580168_61580174dup	NC_000020.10:g.61580167_61580174dup	NC_000020.10:g.61580174_61580175insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC17A9 RefSeqGene	NG_041785.1:g.1158_1176=	NG_041785.1:g.1167_1176del	NG_041785.1:g.1168_1176del	NG_041785.1:g.1169_1176del	NG_041785.1:g.1171_1176del	NG_041785.1:g.1172_1176del	NG_041785.1:g.1173_1176del	NG_041785.1:g.1174_1176del	NG_041785.1:g.1175_1176del	NG_041785.1:g.1176del	NG_041785.1:g.1176dup	NG_041785.1:g.1175_1176dup	NG_041785.1:g.1174_1176dup	NG_041785.1:g.1158_1176T[22]CTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_041785.1:g.1173_1176dup	NG_041785.1:g.1172_1176dup	NG_041785.1:g.1171_1176dup	NG_041785.1:g.1170_1176dup	NG_041785.1:g.1169_1176dup	NG_041785.1:g.1176_1177insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

40 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	MCHAISSO	ss3064862478	Nov 08, 2017 (151)
2	MCHAISSO	ss3065827270	Nov 17, 2017 (151)
3	EVA_DECODE	ss3707302931	Jul 13, 2019 (153)
4	EVA_DECODE	ss3707302932	Jul 13, 2019 (153)
5	EVA_DECODE	ss3707302933	Jul 13, 2019 (153)
6	EVA_DECODE	ss3707302934	Jul 13, 2019 (153)
7	EVA_DECODE	ss3707302935	Jul 13, 2019 (153)
8	EVA_DECODE	ss3707302936	Jul 13, 2019 (153)
9	KHV_HUMAN_GENOMES	ss3822016853	Jul 13, 2019 (153)
10	GNOMAD	ss4356380587	Apr 27, 2021 (155)
11	GNOMAD	ss4356380588	Apr 27, 2021 (155)
12	GNOMAD	ss4356380589	Apr 27, 2021 (155)
13	GNOMAD	ss4356380590	Apr 27, 2021 (155)
14	GNOMAD	ss4356380591	Apr 27, 2021 (155)
15	GNOMAD	ss4356380592	Apr 27, 2021 (155)
16	GNOMAD	ss4356380593	Apr 27, 2021 (155)
17	GNOMAD	ss4356380594	Apr 27, 2021 (155)
18	GNOMAD	ss4356380595	Apr 27, 2021 (155)
19	GNOMAD	ss4356380596	Apr 27, 2021 (155)
20	GNOMAD	ss4356380597	Apr 27, 2021 (155)
21	GNOMAD	ss4356380598	Apr 27, 2021 (155)
22	GNOMAD	ss4356380599	Apr 27, 2021 (155)
23	GNOMAD	ss4356380600	Apr 27, 2021 (155)
24	GNOMAD	ss4356380601	Apr 27, 2021 (155)
25	GNOMAD	ss4356380602	Apr 27, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5309419836	Oct 13, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5309419837	Oct 13, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5309419838	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5309419839	Oct 13, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5309419840	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5501638270	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5501638271	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5501638272	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5501638273	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5501638274	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5790497609	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5790497610	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5790497611	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5790497613	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5790497614	Oct 13, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 556826924 (NC_000020.11:62948803::T 5163/109706) Row 556826925 (NC_000020.11:62948803::TT 44131/109262) Row 556826926 (NC_000020.11:62948803::TTT 1069/109636)...	-	Apr 27, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 124334713 (NC_000020.11:62948803::TT 6678/28234) Row 124334714 (NC_000020.11:62948803:T: 404/28234) Row 124334715 (NC_000020.11:62948803::T 642/28234)...	-	Oct 13, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 124334713 (NC_000020.11:62948803::TT 6678/28234) Row 124334714 (NC_000020.11:62948803:T: 404/28234) Row 124334715 (NC_000020.11:62948803::T 642/28234)...	-	Oct 13, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 124334713 (NC_000020.11:62948803::TT 6678/28234) Row 124334714 (NC_000020.11:62948803:T: 404/28234) Row 124334715 (NC_000020.11:62948803::T 642/28234)...	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 124334713 (NC_000020.11:62948803::TT 6678/28234) Row 124334714 (NC_000020.11:62948803:T: 404/28234) Row 124334715 (NC_000020.11:62948803::T 642/28234)...	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 124334713 (NC_000020.11:62948803::TT 6678/28234) Row 124334714 (NC_000020.11:62948803:T: 404/28234) Row 124334715 (NC_000020.11:62948803::T 642/28234)...	-	Oct 13, 2022 (156)
63	ALFA	NC_000020.11 - 62948804	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).

Associated ID	History Updated (Build)
rs11475889	Oct 07, 2004 (123)
rs369059594	May 15, 2013 (138)
rs386394212	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4356380602	NC_000020.11:62948803:TTTTTTTT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4356380601	NC_000020.11:62948803:TTTTTT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4356380600, ss5790497614	NC_000020.11:62948803:TTTTT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4356380599	NC_000020.11:62948803:TTTT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4356380598, ss5309419840	NC_000020.11:62948803:TTT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3065827270, ss3707302931, ss4356380597, ss5501638273	NC_000020.11:62948803:TT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3822016853, ss5309419837, ss5501638270, ss5790497610	NC_000020.11:62948803:T:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3707302932	NC_000020.11:62948804:T:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4356380587, ss5309419838, ss5501638271, ss5790497611	NC_000020.11:62948803::T	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3707302933	NC_000020.11:62948805::T	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3064862478, ss4356380588, ss5309419836, ss5501638272, ss5790497609	NC_000020.11:62948803::TT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3707302934	NC_000020.11:62948805::TT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380589, ss5309419839, ss5501638274, ss5790497613	NC_000020.11:62948803::TTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3707302935	NC_000020.11:62948805::TTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380595	NC_000020.11:62948803::TTTTTTTTTTT… NC_000020.11:62948803::TTTTTTTTTTTTTTTTTTTTTTCTTTTAATTTACTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTTTTAATTTACTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380590	NC_000020.11:62948803::TTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5148150290	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380591	NC_000020.11:62948803::TTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380592	NC_000020.11:62948803::TTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380593	NC_000020.11:62948803::TTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380594	NC_000020.11:62948803::TTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3707302936	NC_000020.11:62948805::TTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4356380596	NC_000020.11:62948803::TTTTTTTTTTT… NC_000020.11:62948803::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss295057421	NC_000020.9:61050601::TT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	rs2122814133
ss295057422	NC_000020.9:61050618::TT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	rs2122814133
ss947407300, ss5230443261	NC_000020.10:61580155::T	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	rs2122814138
ss664488370, ss1709425814, ss1709425908, ss3788694107, ss3793578013, ss3798465427, ss3835762535, ss5230443262	NC_000020.10:61580155::TT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	rs2122814138
ss1709425816, ss1709425909, ss5230443264	NC_000020.10:61580155::TTT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	rs2122814138
78957577, ss1378589896, ss3018466841, ss5230443263	NC_000020.10:61580155:T:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	rs2122814138
ss5230443265	NC_000020.10:61580155:TTTTT:	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	rs2122814138
ss41422730, ss41430338	NT_011333.6:316786::T	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	rs2122814184
ss80945604, ss95744898	NT_011333.6:316805::TT	NC_000020.11:62948803:TTTTTTTTTTTT… NC_000020.11:62948803:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	rs2122814184

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

No publications for rs11370226

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
Top▲ Help
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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11370226