Name: rs372308686
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.

rs372308686

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:46501663-46501687 (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(GT)₄ / del(GT)₃ / delGTGT / de…
del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupGT=0.10138 (1163/11472, ALFA)
dupGT=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF674 : 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	11472	TGTGTGTGTGTGTGTGTGTGTGTGT=0.89758	TGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.10138, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00105, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000	0.859389	0.062183	0.078428	32
European	Sub	8596	TGTGTGTGTGTGTGTGTGTGTGTGT=0.8638	TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1348, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0014, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.81269	0.082575	0.104735	32
African	Sub	1982	TGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	82	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1900	TGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	76	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	62	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	70	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	382	TGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	308	TGTGTGTGTGTGTGTGTGTGTGTGT=0.987	TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.013, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	0.987013	0.012987	0.0	32

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	11472	(TG)₁₂T=0.89758	del(GT)₄=0.00000, del(GT)₃=0.00000, delGTGT=0.00000, delGT=0.00000, dupGT=0.10138, dupGTGT=0.00105, dup(GT)₃=0.00000, dup(GT)₄=0.00000, dup(GT)₅=0.00000, dup(GT)₆=0.00000, dup(GT)₇=0.00000, dup(GT)₈=0.00000, dup(GT)₉=0.00000, dup(GT)₁₀=0.00000
Allele Frequency Aggregator	European	Sub	8596	(TG)₁₂T=0.8638	del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.1348, dupGTGT=0.0014, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	1982	(TG)₁₂T=1.0000	del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	382	(TG)₁₂T=1.000	del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	308	(TG)₁₂T=0.987	del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.013, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Asian	Sub	76	(TG)₁₂T=1.00	del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	Latin American 1	Sub	70	(TG)₁₂T=1.00	del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(TG)₁₂T=1.00	del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupGT=0.20

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 X	NC_000023.11:g.46501664GT[8]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[9]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[10]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[11]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[13]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[14]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[15]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[16]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[17]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[18]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[19]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[20]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[21]
GRCh38.p14 chr X	NC_000023.11:g.46501664GT[22]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[8]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[9]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[10]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[11]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[13]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[14]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[15]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[16]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[17]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[18]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[19]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[20]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[21]
GRCh37.p13 chr X	NC_000023.10:g.46361099GT[22]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[8]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[9]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[10]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[11]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[13]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[14]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[15]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[16]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[17]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[18]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[19]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[20]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[21]
ZNF674 RefSeqGene	NG_023376.2:g.48772CA[22]

Gene: ZNF674, zinc finger protein 674 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF674 transcript variant 1	NM_001039891.3:c.254-351C… NM_001039891.3:c.254-351CA[8]	N/A	Intron Variant
ZNF674 transcript variant 2	NM_001146291.2:c.239-354C… NM_001146291.2:c.239-354CA[8]	N/A	Intron Variant
ZNF674 transcript variant 3	NM_001190417.2:c.239-351C… NM_001190417.2:c.239-351CA[8]	N/A	Intron Variant
ZNF674 transcript variant X1	XM_011543943.4:c.254-354C… XM_011543943.4:c.254-354CA[8]	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	(TG)₁₂T=	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀
GRCh38.p14 chr X	NC_000023.11:g.46501663_46501687=	NC_000023.11:g.46501664GT[8]	NC_000023.11:g.46501664GT[9]	NC_000023.11:g.46501664GT[10]	NC_000023.11:g.46501664GT[11]	NC_000023.11:g.46501664GT[13]	NC_000023.11:g.46501664GT[14]	NC_000023.11:g.46501664GT[15]	NC_000023.11:g.46501664GT[16]	NC_000023.11:g.46501664GT[17]	NC_000023.11:g.46501664GT[18]	NC_000023.11:g.46501664GT[19]	NC_000023.11:g.46501664GT[20]	NC_000023.11:g.46501664GT[21]	NC_000023.11:g.46501664GT[22]
GRCh37.p13 chr X	NC_000023.10:g.46361098_46361122=	NC_000023.10:g.46361099GT[8]	NC_000023.10:g.46361099GT[9]	NC_000023.10:g.46361099GT[10]	NC_000023.10:g.46361099GT[11]	NC_000023.10:g.46361099GT[13]	NC_000023.10:g.46361099GT[14]	NC_000023.10:g.46361099GT[15]	NC_000023.10:g.46361099GT[16]	NC_000023.10:g.46361099GT[17]	NC_000023.10:g.46361099GT[18]	NC_000023.10:g.46361099GT[19]	NC_000023.10:g.46361099GT[20]	NC_000023.10:g.46361099GT[21]	NC_000023.10:g.46361099GT[22]
ZNF674 RefSeqGene	NG_023376.2:g.48771_48795=	NG_023376.2:g.48772CA[8]	NG_023376.2:g.48772CA[9]	NG_023376.2:g.48772CA[10]	NG_023376.2:g.48772CA[11]	NG_023376.2:g.48772CA[13]	NG_023376.2:g.48772CA[14]	NG_023376.2:g.48772CA[15]	NG_023376.2:g.48772CA[16]	NG_023376.2:g.48772CA[17]	NG_023376.2:g.48772CA[18]	NG_023376.2:g.48772CA[19]	NG_023376.2:g.48772CA[20]	NG_023376.2:g.48772CA[21]	NG_023376.2:g.48772CA[22]
ZNF674 transcript variant 1	NM_001039891.2:c.254-328=	NM_001039891.2:c.254-351CA[8]	NM_001039891.2:c.254-351CA[9]	NM_001039891.2:c.254-351CA[10]	NM_001039891.2:c.254-351CA[11]	NM_001039891.2:c.254-351CA[13]	NM_001039891.2:c.254-351CA[14]	NM_001039891.2:c.254-351CA[15]	NM_001039891.2:c.254-351CA[16]	NM_001039891.2:c.254-351CA[17]	NM_001039891.2:c.254-351CA[18]	NM_001039891.2:c.254-351CA[19]	NM_001039891.2:c.254-351CA[20]	NM_001039891.2:c.254-351CA[21]	NM_001039891.2:c.254-351CA[22]
ZNF674 transcript variant 1	NM_001039891.3:c.254-328=	NM_001039891.3:c.254-351CA[8]	NM_001039891.3:c.254-351CA[9]	NM_001039891.3:c.254-351CA[10]	NM_001039891.3:c.254-351CA[11]	NM_001039891.3:c.254-351CA[13]	NM_001039891.3:c.254-351CA[14]	NM_001039891.3:c.254-351CA[15]	NM_001039891.3:c.254-351CA[16]	NM_001039891.3:c.254-351CA[17]	NM_001039891.3:c.254-351CA[18]	NM_001039891.3:c.254-351CA[19]	NM_001039891.3:c.254-351CA[20]	NM_001039891.3:c.254-351CA[21]	NM_001039891.3:c.254-351CA[22]
ZNF674 transcript variant 2	NM_001146291.1:c.239-331=	NM_001146291.1:c.239-354CA[8]	NM_001146291.1:c.239-354CA[9]	NM_001146291.1:c.239-354CA[10]	NM_001146291.1:c.239-354CA[11]	NM_001146291.1:c.239-354CA[13]	NM_001146291.1:c.239-354CA[14]	NM_001146291.1:c.239-354CA[15]	NM_001146291.1:c.239-354CA[16]	NM_001146291.1:c.239-354CA[17]	NM_001146291.1:c.239-354CA[18]	NM_001146291.1:c.239-354CA[19]	NM_001146291.1:c.239-354CA[20]	NM_001146291.1:c.239-354CA[21]	NM_001146291.1:c.239-354CA[22]
ZNF674 transcript variant 2	NM_001146291.2:c.239-331=	NM_001146291.2:c.239-354CA[8]	NM_001146291.2:c.239-354CA[9]	NM_001146291.2:c.239-354CA[10]	NM_001146291.2:c.239-354CA[11]	NM_001146291.2:c.239-354CA[13]	NM_001146291.2:c.239-354CA[14]	NM_001146291.2:c.239-354CA[15]	NM_001146291.2:c.239-354CA[16]	NM_001146291.2:c.239-354CA[17]	NM_001146291.2:c.239-354CA[18]	NM_001146291.2:c.239-354CA[19]	NM_001146291.2:c.239-354CA[20]	NM_001146291.2:c.239-354CA[21]	NM_001146291.2:c.239-354CA[22]
ZNF674 transcript variant 3	NM_001190417.1:c.239-328=	NM_001190417.1:c.239-351CA[8]	NM_001190417.1:c.239-351CA[9]	NM_001190417.1:c.239-351CA[10]	NM_001190417.1:c.239-351CA[11]	NM_001190417.1:c.239-351CA[13]	NM_001190417.1:c.239-351CA[14]	NM_001190417.1:c.239-351CA[15]	NM_001190417.1:c.239-351CA[16]	NM_001190417.1:c.239-351CA[17]	NM_001190417.1:c.239-351CA[18]	NM_001190417.1:c.239-351CA[19]	NM_001190417.1:c.239-351CA[20]	NM_001190417.1:c.239-351CA[21]	NM_001190417.1:c.239-351CA[22]
ZNF674 transcript variant 3	NM_001190417.2:c.239-328=	NM_001190417.2:c.239-351CA[8]	NM_001190417.2:c.239-351CA[9]	NM_001190417.2:c.239-351CA[10]	NM_001190417.2:c.239-351CA[11]	NM_001190417.2:c.239-351CA[13]	NM_001190417.2:c.239-351CA[14]	NM_001190417.2:c.239-351CA[15]	NM_001190417.2:c.239-351CA[16]	NM_001190417.2:c.239-351CA[17]	NM_001190417.2:c.239-351CA[18]	NM_001190417.2:c.239-351CA[19]	NM_001190417.2:c.239-351CA[20]	NM_001190417.2:c.239-351CA[21]	NM_001190417.2:c.239-351CA[22]
ZNF674 transcript variant X1	XM_011543943.4:c.254-331=	XM_011543943.4:c.254-354CA[8]	XM_011543943.4:c.254-354CA[9]	XM_011543943.4:c.254-354CA[10]	XM_011543943.4:c.254-354CA[11]	XM_011543943.4:c.254-354CA[13]	XM_011543943.4:c.254-354CA[14]	XM_011543943.4:c.254-354CA[15]	XM_011543943.4:c.254-354CA[16]	XM_011543943.4:c.254-354CA[17]	XM_011543943.4:c.254-354CA[18]	XM_011543943.4:c.254-354CA[19]	XM_011543943.4:c.254-354CA[20]	XM_011543943.4:c.254-354CA[21]	XM_011543943.4:c.254-354CA[22]

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#.

50 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss664568378	Apr 01, 2015 (144)
2	BILGI_BIOE	ss666778198	Apr 25, 2013 (138)
3	SSIP	ss947422411	Aug 21, 2014 (142)
4	DDI	ss1536940159	Apr 01, 2015 (144)
5	1000GENOMES	ss1554309430	Apr 01, 2015 (144)
6	1000GENOMES	ss1554309431	Apr 01, 2015 (144)
7	EVA_GENOME_DK	ss1577559747	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1709719215	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709719217	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709719381	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1709719382	Apr 01, 2015 (144)
12	SWEGEN	ss3019919854	Nov 08, 2017 (151)
13	SWEGEN	ss3019919855	Nov 08, 2017 (151)
14	MCHAISSO	ss3065261507	Nov 08, 2017 (151)
15	KHV_HUMAN_GENOMES	ss3822963565	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3822963566	Jul 13, 2019 (153)
17	EVA	ss3836163439	Apr 27, 2020 (154)
18	EVA	ss3847213588	Apr 27, 2020 (154)
19	GNOMAD	ss4370936425	Apr 26, 2021 (155)
20	GNOMAD	ss4370936426	Apr 26, 2021 (155)
21	GNOMAD	ss4370936427	Apr 26, 2021 (155)
22	GNOMAD	ss4370936428	Apr 26, 2021 (155)
23	GNOMAD	ss4370936429	Apr 26, 2021 (155)
24	GNOMAD	ss4370936430	Apr 26, 2021 (155)
25	GNOMAD	ss4370936431	Apr 26, 2021 (155)
26	GNOMAD	ss4370936432	Apr 26, 2021 (155)
27	GNOMAD	ss4370936433	Apr 26, 2021 (155)
28	GNOMAD	ss4370936435	Apr 26, 2021 (155)
29	GNOMAD	ss4370936436	Apr 26, 2021 (155)
30	GNOMAD	ss4370936437	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5234328170	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5234328171	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5234328172	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5234328173	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5312443048	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5312443049	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5312443050	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5312443051	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5312443052	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5504123592	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5504123593	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5504123594	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5504123595	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5504123596	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5504123597	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5795993606	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5795993607	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5795993608	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5795993610	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5795993611	Oct 16, 2022 (156)
51	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 45435811 (NC_000023.10:46361097::TG 931/2889) Row 45435812 (NC_000023.10:46361097::TGTG 95/2889)	-	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 45435811 (NC_000023.10:46361097::TG 931/2889) Row 45435812 (NC_000023.10:46361097::TGTG 95/2889)	-	Oct 12, 2018 (152)
53	The Danish reference pan genome	NC_000023.10 - 46361098	Apr 27, 2020 (154)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579927538 (NC_000023.11:46501662::TG 22535/94988) Row 579927539 (NC_000023.11:46501662::TGTG 1630/95130) Row 579927540 (NC_000023.11:46501662::TGTGTG 22/95156)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 92297477 (NC_000023.10:46361097::TG 1425/12842) Row 92297478 (NC_000023.10:46361097:TG: 20/12842) Row 92297479 (NC_000023.10:46361097::TGTG 53/12842)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 92297477 (NC_000023.10:46361097::TG 1425/12842) Row 92297478 (NC_000023.10:46361097:TG: 20/12842) Row 92297479 (NC_000023.10:46361097::TGTG 53/12842)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 92297477 (NC_000023.10:46361097::TG 1425/12842) Row 92297478 (NC_000023.10:46361097:TG: 20/12842) Row 92297479 (NC_000023.10:46361097::TGTG 53/12842)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 92297477 (NC_000023.10:46361097::TG 1425/12842) Row 92297478 (NC_000023.10:46361097:TG: 20/12842) Row 92297479 (NC_000023.10:46361097::TGTG 53/12842)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 129830710 (NC_000023.11:46501662::TG 2406/22222) Row 129830711 (NC_000023.11:46501662::TGTG 104/22222) Row 129830712 (NC_000023.11:46501662:TG: 20/22222)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 129830710 (NC_000023.11:46501662::TG 2406/22222) Row 129830711 (NC_000023.11:46501662::TGTG 104/22222) Row 129830712 (NC_000023.11:46501662:TG: 20/22222)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 129830710 (NC_000023.11:46501662::TG 2406/22222) Row 129830711 (NC_000023.11:46501662::TGTG 104/22222) Row 129830712 (NC_000023.11:46501662:TG: 20/22222)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 129830710 (NC_000023.11:46501662::TG 2406/22222) Row 129830711 (NC_000023.11:46501662::TGTG 104/22222) Row 129830712 (NC_000023.11:46501662:TG: 20/22222)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 129830710 (NC_000023.11:46501662::TG 2406/22222) Row 129830711 (NC_000023.11:46501662::TGTG 104/22222) Row 129830712 (NC_000023.11:46501662:TG: 20/22222)...	-	Oct 16, 2022 (156)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 45435811 (NC_000023.10:46361097::TG 1175/3708) Row 45435812 (NC_000023.10:46361097::TGTG 126/3708)	-	Oct 12, 2018 (152)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 45435811 (NC_000023.10:46361097::TG 1175/3708) Row 45435812 (NC_000023.10:46361097::TGTG 126/3708)	-	Oct 12, 2018 (152)
77	ALFA	NC_000023.11 - 46501663	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)
rs368622560	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
ss4370936437	NC_000023.11:46501662:TGTGTG:	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss5234328173	NC_000023.10:46361097:TGTG:	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936436, ss5795993610	NC_000023.11:46501662:TGTG:	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3836163439, ss5234328171	NC_000023.10:46361097:TG:	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936435, ss5312443050, ss5504123593, ss5795993608	NC_000023.11:46501662:TG:	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
1324503, ss664568378, ss666778198, ss947422411, ss1536940159, ss1554309430, ss1577559747, ss1709719215, ss1709719381, ss3019919854, ss5234328170	NC_000023.10:46361097::TG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065261507, ss3822963565, ss3847213588, ss4370936425, ss5312443048, ss5504123592, ss5795993606	NC_000023.11:46501662::TG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1554309431, ss1709719217, ss1709719382, ss3019919855, ss5234328172	NC_000023.10:46361097::TGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3822963566, ss4370936426, ss5312443049, ss5504123594, ss5795993607	NC_000023.11:46501662::TGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936427, ss5504123595, ss5795993611	NC_000023.11:46501662::TGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936428	NC_000023.11:46501662::TGTGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936429, ss5312443052, ss5504123596	NC_000023.11:46501662::TGTGTGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936430, ss5312443051, ss5504123597	NC_000023.11:46501662::TGTGTGTGTGT… NC_000023.11:46501662::TGTGTGTGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936431	NC_000023.11:46501662::TGTGTGTGTGT… NC_000023.11:46501662::TGTGTGTGTGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936432	NC_000023.11:46501662::TGTGTGTGTGT… NC_000023.11:46501662::TGTGTGTGTGTGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4370936433	NC_000023.11:46501662::TGTGTGTGTGT… NC_000023.11:46501662::TGTGTGTGTGTGTGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
5582159245	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3610118158	NC_000023.11:46501662::TGTGTGTG	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
ss3610118169	NC_000023.11:46501662:TGTGTGTG:	NC_000023.11:46501662:TGTGTGTGTGTG… NC_000023.11:46501662:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT

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

No publications for rs372308686

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).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs372308686