Name: rs34021774
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.

rs34021774

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:40030667-40030676 (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)₄ / delTT / delT / dupT / du…
del(T)₄ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00311 (42/13501, ALFA)
dupTT=0.0022 (4/1816, Korea1K)
dupT=0.002 (1/592, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MED24 : 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	13501	TTTTTTTTTT=0.99682	TTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00311, TTTTTTTTTTTT=0.00007, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000	0.996324	0.00016	0.003516	22
European	Sub	10277	TTTTTTTTTT=0.99582	TTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00409, TTTTTTTTTTTT=0.00010, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000	0.99505	0.000215	0.004735	17
African	Sub	1858	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	74	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1784	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	108	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	140	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	594	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	94	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	430	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13501	(T)₁₀=0.99682	del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00311, dupTT=0.00007, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000
Allele Frequency Aggregator	European	Sub	10277	(T)₁₀=0.99582	del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00409, dupTT=0.00010, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000
Allele Frequency Aggregator	African	Sub	1858	(T)₁₀=1.0000	del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	594	(T)₁₀=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	430	(T)₁₀=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	140	(T)₁₀=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Asian	Sub	108	(T)₁₀=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(T)₁₀=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Korean Genome Project	KOREAN	Study-wide	1816	- No frequency provided	dupTT=0.0022
Northern Sweden	ACPOP	Study-wide	592	- No frequency provided	dupT=0.002

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 17	NC_000017.11:g.40030673_40030676del
GRCh38.p14 chr 17	NC_000017.11:g.40030675_40030676del
GRCh38.p14 chr 17	NC_000017.11:g.40030676del
GRCh38.p14 chr 17	NC_000017.11:g.40030676dup
GRCh38.p14 chr 17	NC_000017.11:g.40030675_40030676dup
GRCh38.p14 chr 17	NC_000017.11:g.40030674_40030676dup
GRCh38.p14 chr 17	NC_000017.11:g.40030673_40030676dup
GRCh38.p14 chr 17	NC_000017.11:g.40030672_40030676dup
GRCh38.p14 chr 17	NC_000017.11:g.40030671_40030676dup
GRCh37.p13 chr 17	NC_000017.10:g.38186926_38186929del
GRCh37.p13 chr 17	NC_000017.10:g.38186928_38186929del
GRCh37.p13 chr 17	NC_000017.10:g.38186929del
GRCh37.p13 chr 17	NC_000017.10:g.38186929dup
GRCh37.p13 chr 17	NC_000017.10:g.38186928_38186929dup
GRCh37.p13 chr 17	NC_000017.10:g.38186927_38186929dup
GRCh37.p13 chr 17	NC_000017.10:g.38186926_38186929dup
GRCh37.p13 chr 17	NC_000017.10:g.38186925_38186929dup
GRCh37.p13 chr 17	NC_000017.10:g.38186924_38186929dup

Gene: MED24, mediator complex subunit 24 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MED24 transcript variant 2	NM_001079518.2:c.1115+489… NM_001079518.2:c.1115+489_1115+492del	N/A	Intron Variant
MED24 transcript variant 3	NM_001267797.2:c.1115+489… NM_001267797.2:c.1115+489_1115+492del	N/A	Intron Variant
MED24 transcript variant 5	NM_001330211.2:c.1211+489… NM_001330211.2:c.1211+489_1211+492del	N/A	Intron Variant
MED24 transcript variant 1	NM_014815.4:c.1154+489_11… NM_014815.4:c.1154+489_1154+492del	N/A	Intron Variant
MED24 transcript variant 4	NR_052017.2: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	(T)₁₀=	del(T)₄	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆
GRCh38.p14 chr 17	NC_000017.11:g.40030667_40030676=	NC_000017.11:g.40030673_40030676del	NC_000017.11:g.40030675_40030676del	NC_000017.11:g.40030676del	NC_000017.11:g.40030676dup	NC_000017.11:g.40030675_40030676dup	NC_000017.11:g.40030674_40030676dup	NC_000017.11:g.40030673_40030676dup	NC_000017.11:g.40030672_40030676dup	NC_000017.11:g.40030671_40030676dup
GRCh37.p13 chr 17	NC_000017.10:g.38186920_38186929=	NC_000017.10:g.38186926_38186929del	NC_000017.10:g.38186928_38186929del	NC_000017.10:g.38186929del	NC_000017.10:g.38186929dup	NC_000017.10:g.38186928_38186929dup	NC_000017.10:g.38186927_38186929dup	NC_000017.10:g.38186926_38186929dup	NC_000017.10:g.38186925_38186929dup	NC_000017.10:g.38186924_38186929dup
MED24 transcript variant 2	NM_001079518.1:c.1115+492=	NM_001079518.1:c.1115+489_1115+492del	NM_001079518.1:c.1115+491_1115+492del	NM_001079518.1:c.1115+492del	NM_001079518.1:c.1115+492dup	NM_001079518.1:c.1115+491_1115+492dup	NM_001079518.1:c.1115+490_1115+492dup	NM_001079518.1:c.1115+489_1115+492dup	NM_001079518.1:c.1115+488_1115+492dup	NM_001079518.1:c.1115+487_1115+492dup
MED24 transcript variant 2	NM_001079518.2:c.1115+492=	NM_001079518.2:c.1115+489_1115+492del	NM_001079518.2:c.1115+491_1115+492del	NM_001079518.2:c.1115+492del	NM_001079518.2:c.1115+492dup	NM_001079518.2:c.1115+491_1115+492dup	NM_001079518.2:c.1115+490_1115+492dup	NM_001079518.2:c.1115+489_1115+492dup	NM_001079518.2:c.1115+488_1115+492dup	NM_001079518.2:c.1115+487_1115+492dup
MED24 transcript variant 3	NM_001267797.1:c.1115+492=	NM_001267797.1:c.1115+489_1115+492del	NM_001267797.1:c.1115+491_1115+492del	NM_001267797.1:c.1115+492del	NM_001267797.1:c.1115+492dup	NM_001267797.1:c.1115+491_1115+492dup	NM_001267797.1:c.1115+490_1115+492dup	NM_001267797.1:c.1115+489_1115+492dup	NM_001267797.1:c.1115+488_1115+492dup	NM_001267797.1:c.1115+487_1115+492dup
MED24 transcript variant 3	NM_001267797.2:c.1115+492=	NM_001267797.2:c.1115+489_1115+492del	NM_001267797.2:c.1115+491_1115+492del	NM_001267797.2:c.1115+492del	NM_001267797.2:c.1115+492dup	NM_001267797.2:c.1115+491_1115+492dup	NM_001267797.2:c.1115+490_1115+492dup	NM_001267797.2:c.1115+489_1115+492dup	NM_001267797.2:c.1115+488_1115+492dup	NM_001267797.2:c.1115+487_1115+492dup
MED24 transcript variant 5	NM_001330211.2:c.1211+492=	NM_001330211.2:c.1211+489_1211+492del	NM_001330211.2:c.1211+491_1211+492del	NM_001330211.2:c.1211+492del	NM_001330211.2:c.1211+492dup	NM_001330211.2:c.1211+491_1211+492dup	NM_001330211.2:c.1211+490_1211+492dup	NM_001330211.2:c.1211+489_1211+492dup	NM_001330211.2:c.1211+488_1211+492dup	NM_001330211.2:c.1211+487_1211+492dup
MED24 transcript variant 1	NM_014815.3:c.1154+492=	NM_014815.3:c.1154+489_1154+492del	NM_014815.3:c.1154+491_1154+492del	NM_014815.3:c.1154+492del	NM_014815.3:c.1154+492dup	NM_014815.3:c.1154+491_1154+492dup	NM_014815.3:c.1154+490_1154+492dup	NM_014815.3:c.1154+489_1154+492dup	NM_014815.3:c.1154+488_1154+492dup	NM_014815.3:c.1154+487_1154+492dup
MED24 transcript variant 1	NM_014815.4:c.1154+492=	NM_014815.4:c.1154+489_1154+492del	NM_014815.4:c.1154+491_1154+492del	NM_014815.4:c.1154+492del	NM_014815.4:c.1154+492dup	NM_014815.4:c.1154+491_1154+492dup	NM_014815.4:c.1154+490_1154+492dup	NM_014815.4:c.1154+489_1154+492dup	NM_014815.4:c.1154+488_1154+492dup	NM_014815.4:c.1154+487_1154+492dup
MED24 transcript variant X1	XM_005257869.1:c.1286+492=	XM_005257869.1:c.1286+489_1286+492del	XM_005257869.1:c.1286+491_1286+492del	XM_005257869.1:c.1286+492del	XM_005257869.1:c.1286+492dup	XM_005257869.1:c.1286+491_1286+492dup	XM_005257869.1:c.1286+490_1286+492dup	XM_005257869.1:c.1286+489_1286+492dup	XM_005257869.1:c.1286+488_1286+492dup	XM_005257869.1:c.1286+487_1286+492dup
MED24 transcript variant X2	XM_005257870.1:c.1229+492=	XM_005257870.1:c.1229+489_1229+492del	XM_005257870.1:c.1229+491_1229+492del	XM_005257870.1:c.1229+492del	XM_005257870.1:c.1229+492dup	XM_005257870.1:c.1229+491_1229+492dup	XM_005257870.1:c.1229+490_1229+492dup	XM_005257870.1:c.1229+489_1229+492dup	XM_005257870.1:c.1229+488_1229+492dup	XM_005257870.1:c.1229+487_1229+492dup
MED24 transcript variant X3	XM_005257871.1:c.1211+492=	XM_005257871.1:c.1211+489_1211+492del	XM_005257871.1:c.1211+491_1211+492del	XM_005257871.1:c.1211+492del	XM_005257871.1:c.1211+492dup	XM_005257871.1:c.1211+491_1211+492dup	XM_005257871.1:c.1211+490_1211+492dup	XM_005257871.1:c.1211+489_1211+492dup	XM_005257871.1:c.1211+488_1211+492dup	XM_005257871.1:c.1211+487_1211+492dup
MED24 transcript variant X4	XM_005257872.1:c.1286+492=	XM_005257872.1:c.1286+489_1286+492del	XM_005257872.1:c.1286+491_1286+492del	XM_005257872.1:c.1286+492del	XM_005257872.1:c.1286+492dup	XM_005257872.1:c.1286+491_1286+492dup	XM_005257872.1:c.1286+490_1286+492dup	XM_005257872.1:c.1286+489_1286+492dup	XM_005257872.1:c.1286+488_1286+492dup	XM_005257872.1:c.1286+487_1286+492dup
MED24 transcript variant X5	XM_005257873.1:c.1286+492=	XM_005257873.1:c.1286+489_1286+492del	XM_005257873.1:c.1286+491_1286+492del	XM_005257873.1:c.1286+492del	XM_005257873.1:c.1286+492dup	XM_005257873.1:c.1286+491_1286+492dup	XM_005257873.1:c.1286+490_1286+492dup	XM_005257873.1:c.1286+489_1286+492dup	XM_005257873.1:c.1286+488_1286+492dup	XM_005257873.1:c.1286+487_1286+492dup
MED24 transcript variant X12	XM_005257874.1:c.1229+492=	XM_005257874.1:c.1229+489_1229+492del	XM_005257874.1:c.1229+491_1229+492del	XM_005257874.1:c.1229+492del	XM_005257874.1:c.1229+492dup	XM_005257874.1:c.1229+491_1229+492dup	XM_005257874.1:c.1229+490_1229+492dup	XM_005257874.1:c.1229+489_1229+492dup	XM_005257874.1:c.1229+488_1229+492dup	XM_005257874.1:c.1229+487_1229+492dup
MED24 transcript variant X7	XM_005257875.1:c.1061+492=	XM_005257875.1:c.1061+489_1061+492del	XM_005257875.1:c.1061+491_1061+492del	XM_005257875.1:c.1061+492del	XM_005257875.1:c.1061+492dup	XM_005257875.1:c.1061+491_1061+492dup	XM_005257875.1:c.1061+490_1061+492dup	XM_005257875.1:c.1061+489_1061+492dup	XM_005257875.1:c.1061+488_1061+492dup	XM_005257875.1:c.1061+487_1061+492dup
MED24 transcript variant X8	XM_005257876.1:c.1190+492=	XM_005257876.1:c.1190+489_1190+492del	XM_005257876.1:c.1190+491_1190+492del	XM_005257876.1:c.1190+492del	XM_005257876.1:c.1190+492dup	XM_005257876.1:c.1190+491_1190+492dup	XM_005257876.1:c.1190+490_1190+492dup	XM_005257876.1:c.1190+489_1190+492dup	XM_005257876.1:c.1190+488_1190+492dup	XM_005257876.1:c.1190+487_1190+492dup
MED24 transcript variant X9	XM_005257877.1:c.884+492=	XM_005257877.1:c.884+489_884+492del	XM_005257877.1:c.884+491_884+492del	XM_005257877.1:c.884+492del	XM_005257877.1:c.884+492dup	XM_005257877.1:c.884+491_884+492dup	XM_005257877.1:c.884+490_884+492dup	XM_005257877.1:c.884+489_884+492dup	XM_005257877.1:c.884+488_884+492dup	XM_005257877.1:c.884+487_884+492dup

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#.

29 SubSNP, 13 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40854805	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95693604	Feb 13, 2009 (130)
3	BUSHMAN	ss193447877	Jul 04, 2010 (132)
4	SWEGEN	ss3015506222	Nov 08, 2017 (151)
5	SWEGEN	ss3015506223	Nov 08, 2017 (151)
6	MCHAISSO	ss3063867270	Nov 08, 2017 (151)
7	MCHAISSO	ss3064710764	Nov 08, 2017 (151)
8	EVA_DECODE	ss3700432806	Jul 13, 2019 (153)
9	EVA_DECODE	ss3700432807	Jul 13, 2019 (153)
10	EVA_DECODE	ss3700432808	Jul 13, 2019 (153)
11	EVA_DECODE	ss3700432809	Jul 13, 2019 (153)
12	EVA_DECODE	ss3700432811	Jul 13, 2019 (153)
13	ACPOP	ss3742012424	Jul 13, 2019 (153)
14	KOGIC	ss3978812141	Apr 27, 2020 (154)
15	GNOMAD	ss4311274832	Apr 26, 2021 (155)
16	GNOMAD	ss4311274833	Apr 26, 2021 (155)
17	GNOMAD	ss4311274834	Apr 26, 2021 (155)
18	GNOMAD	ss4311274836	Apr 26, 2021 (155)
19	GNOMAD	ss4311274837	Apr 26, 2021 (155)
20	GNOMAD	ss4311274839	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5222333955	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5222333956	Apr 26, 2021 (155)
23	HUGCELL_USP	ss5496136897	Oct 16, 2022 (156)
24	HUGCELL_USP	ss5496136898	Oct 16, 2022 (156)
25	HUGCELL_USP	ss5496136899	Oct 16, 2022 (156)
26	HUGCELL_USP	ss5496136900	Oct 16, 2022 (156)
27	TOMMO_GENOMICS	ss5778514994	Oct 16, 2022 (156)
28	TOMMO_GENOMICS	ss5778514995	Oct 16, 2022 (156)
29	EVA	ss5833960262	Oct 16, 2022 (156)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506740190 (NC_000017.11:40030666::T 516/119462) Row 506740191 (NC_000017.11:40030666::TT 7731/119398) Row 506740192 (NC_000017.11:40030666::TTT 344/119466)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506740190 (NC_000017.11:40030666::T 516/119462) Row 506740191 (NC_000017.11:40030666::TT 7731/119398) Row 506740192 (NC_000017.11:40030666::TTT 344/119466)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506740190 (NC_000017.11:40030666::T 516/119462) Row 506740191 (NC_000017.11:40030666::TT 7731/119398) Row 506740192 (NC_000017.11:40030666::TTT 344/119466)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506740190 (NC_000017.11:40030666::T 516/119462) Row 506740191 (NC_000017.11:40030666::TT 7731/119398) Row 506740192 (NC_000017.11:40030666::TTT 344/119466)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506740190 (NC_000017.11:40030666::T 516/119462) Row 506740191 (NC_000017.11:40030666::TT 7731/119398) Row 506740192 (NC_000017.11:40030666::TTT 344/119466)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506740190 (NC_000017.11:40030666::T 516/119462) Row 506740191 (NC_000017.11:40030666::TT 7731/119398) Row 506740192 (NC_000017.11:40030666::TTT 344/119466)...	-	Apr 26, 2021 (155)
36	Korean Genome Project	NC_000017.11 - 40030668	Apr 27, 2020 (154)
37	Northern Sweden	NC_000017.10 - 38186920	Jul 13, 2019 (153)
38	8.3KJPN Submission ignored due to conflicting rows: Row 80303262 (NC_000017.10:38186919::T 3/15878) Row 80303263 (NC_000017.10:38186919::TT 34/15878)	-	Apr 26, 2021 (155)
39	8.3KJPN Submission ignored due to conflicting rows: Row 80303262 (NC_000017.10:38186919::T 3/15878) Row 80303263 (NC_000017.10:38186919::TT 34/15878)	-	Apr 26, 2021 (155)
40	14KJPN Submission ignored due to conflicting rows: Row 112352098 (NC_000017.11:40030666::TT 61/28258) Row 112352099 (NC_000017.11:40030666::T 4/28258)	-	Oct 16, 2022 (156)
41	14KJPN Submission ignored due to conflicting rows: Row 112352098 (NC_000017.11:40030666::TT 61/28258) Row 112352099 (NC_000017.11:40030666::T 4/28258)	-	Oct 16, 2022 (156)
42	ALFA	NC_000017.11 - 40030667	Apr 26, 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)
rs34557509	May 23, 2006 (127)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4311274839	NC_000017.11:40030666:TTTT:	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTT	(self)
ss3700432806	NC_000017.11:40030666:TT:	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTT	(self)
ss3700432807	NC_000017.11:40030667:T:	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTT	(self)
15297289, ss3015506222, ss3742012424, ss5222333955	NC_000017.10:38186919::T	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3063867270, ss3064710764, ss4311274832, ss5496136898, ss5778514995	NC_000017.11:40030666::T	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3700432808	NC_000017.11:40030668::T	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3015506223, ss5222333956, ss5833960262	NC_000017.10:38186919::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4311274833, ss5496136897, ss5778514994	NC_000017.11:40030666::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
35190142, ss3978812141	NC_000017.11:40030667::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3700432809, ss3700432811	NC_000017.11:40030668::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss40854805	NT_010783.15:3461071::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss95693604	NT_010783.15:3461081::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss193447877	NT_010783.16:13094686::TT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4311274834, ss5496136899	NC_000017.11:40030666::TTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4311274836, ss5496136900	NC_000017.11:40030666::TTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4311274837	NC_000017.11:40030666::TTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2473406479	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3262361134	NC_000017.11:40030666:T:	NC_000017.11:40030666:TTTTTTTTTT:T… NC_000017.11:40030666:TTTTTTTTTT:TTTTTTTTT

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

No publications for rs34021774

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

rs34021774