Name: rs373178468
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.

rs373178468

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:69555237-69555260 (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)₆ / del(GT)₅ / del(GT)₄ / d…
del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅
Variation Type: Indel Insertion and Deletion
Frequency: delGT=0.4647 (2511/5404, ALFA)
delGT=0.467 (253/542, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OCLN : 3 Prime UTR 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	5404	GTGTGTGTGTGTGTGTGTGTGTGT=0.5337	GTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0013, GTGTGTGTGTGTGTGTGTGTGT=0.4647, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0004, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.312291	0.242481	0.445228	16
European	Sub	4578	GTGTGTGTGTGTGTGTGTGTGTGT=0.4506	GTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0015, GTGTGTGTGTGTGTGTGTGTGT=0.5474, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0004, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.189474	0.285965	0.524561	5
African	Sub	708	GTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	36	GTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	672	GTGTGTGTGTGTGTGTGTGTGTGT=1.000	GTGTGTGTGTGT=0.000, GTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	GTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	GTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	GTGTGTGTGTGTGTGTGTGTGTGT=0	GTGTGTGTGTGT=0, GTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 1	Sub	12	GTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	58	GTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	GTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other	Sub	38	GTGTGTGTGTGTGTGTGTGTGTGT=0.87	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.13, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	0.789474	0.052632	0.157895	1

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	5404	(GT)₁₂=0.5337	del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0013, delGT=0.4647, dupGT=0.0004, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	European	Sub	4578	(GT)₁₂=0.4506	del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0015, delGT=0.5474, dupGT=0.0004, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	African	Sub	708	(GT)₁₂=1.000	del(GT)₆=0.000, del(GT)₅=0.000, 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
Allele Frequency Aggregator	Latin American 2	Sub	58	(GT)₁₂=1.00	del(GT)₆=0.00, del(GT)₅=0.00, 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
Allele Frequency Aggregator	Other	Sub	38	(GT)₁₂=0.87	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.13, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(GT)₁₂=1.00	del(GT)₆=0.00, del(GT)₅=0.00, 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
Allele Frequency Aggregator	Asian	Sub	6	(GT)₁₂=1.0	del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(GT)₁₂=1.0	del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0
Northern Sweden	ACPOP	Study-wide	542	(GT)₁₂=0.533	delGT=0.467

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 5	NC_000005.10:g.69555237GT[6]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[7]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[8]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[9]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[10]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[11]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[13]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[14]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[15]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[16]
GRCh38.p14 chr 5	NC_000005.10:g.69555237GT[17]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[6]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[7]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[8]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[9]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[10]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[11]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[13]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[14]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[15]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[16]
GRCh37.p13 chr 5	NC_000005.9:g.68851064GT[17]
OCLN RefSeqGene	NG_028291.1:g.67946GT[6]
OCLN RefSeqGene	NG_028291.1:g.67946GT[7]
OCLN RefSeqGene	NG_028291.1:g.67946GT[8]
OCLN RefSeqGene	NG_028291.1:g.67946GT[9]
OCLN RefSeqGene	NG_028291.1:g.67946GT[10]
OCLN RefSeqGene	NG_028291.1:g.67946GT[11]
OCLN RefSeqGene	NG_028291.1:g.67946GT[13]
OCLN RefSeqGene	NG_028291.1:g.67946GT[14]
OCLN RefSeqGene	NG_028291.1:g.67946GT[15]
OCLN RefSeqGene	NG_028291.1:g.67946GT[16]
OCLN RefSeqGene	NG_028291.1:g.67946GT[17]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[6]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[7]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[8]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[9]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[10]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[11]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[13]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[14]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[15]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[16]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180GT[17]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[12]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[6]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[7]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[8]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[9]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[10]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[13]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[14]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[15]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[16]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[17]

Gene: OCLN, occludin (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OCLN transcript variant 3	NM_001205255.1:c.1566_1… NM_001205255.1:c.1566_1589=	N/A	3 Prime UTR Variant
OCLN transcript variant 2	NM_001205254.2:c.1566_1… NM_001205254.2:c.1566_1589=	N/A	3 Prime UTR Variant
OCLN transcript variant 1	NM_002538.4:c.1566_1589=	N/A	3 Prime UTR Variant
OCLN transcript variant X1	XM_047416593.1:c.1566_1… XM_047416593.1:c.1566_1589=	N/A	3 Prime UTR Variant
OCLN transcript variant X2	XM_047416594.1:c.1566_1… XM_047416594.1:c.1566_1589=	N/A	3 Prime UTR Variant
OCLN transcript variant X3	XM_017008913.3:c.1566_1… XM_017008913.3:c.1566_1589=	N/A	3 Prime UTR Variant
OCLN transcript variant X4	XM_017008914.3:c.1566_1… XM_017008914.3:c.1566_1589=	N/A	3 Prime UTR 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	(GT)₁₂=	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅
GRCh38.p14 chr 5	NC_000005.10:g.69555237_69555260=	NC_000005.10:g.69555237GT[6]	NC_000005.10:g.69555237GT[7]	NC_000005.10:g.69555237GT[8]	NC_000005.10:g.69555237GT[9]	NC_000005.10:g.69555237GT[10]	NC_000005.10:g.69555237GT[11]	NC_000005.10:g.69555237GT[13]	NC_000005.10:g.69555237GT[14]	NC_000005.10:g.69555237GT[15]	NC_000005.10:g.69555237GT[16]	NC_000005.10:g.69555237GT[17]
GRCh37.p13 chr 5	NC_000005.9:g.68851064_68851087=	NC_000005.9:g.68851064GT[6]	NC_000005.9:g.68851064GT[7]	NC_000005.9:g.68851064GT[8]	NC_000005.9:g.68851064GT[9]	NC_000005.9:g.68851064GT[10]	NC_000005.9:g.68851064GT[11]	NC_000005.9:g.68851064GT[13]	NC_000005.9:g.68851064GT[14]	NC_000005.9:g.68851064GT[15]	NC_000005.9:g.68851064GT[16]	NC_000005.9:g.68851064GT[17]
OCLN RefSeqGene	NG_028291.1:g.67946_67969=	NG_028291.1:g.67946GT[6]	NG_028291.1:g.67946GT[7]	NG_028291.1:g.67946GT[8]	NG_028291.1:g.67946GT[9]	NG_028291.1:g.67946GT[10]	NG_028291.1:g.67946GT[11]	NG_028291.1:g.67946GT[13]	NG_028291.1:g.67946GT[14]	NG_028291.1:g.67946GT[15]	NG_028291.1:g.67946GT[16]	NG_028291.1:g.67946GT[17]
OCLN transcript variant 1	NM_002538.4:c.1566_1589=	NM_002538.4:c.*1566GT[6]	NM_002538.4:c.*1566GT[7]	NM_002538.4:c.*1566GT[8]	NM_002538.4:c.*1566GT[9]	NM_002538.4:c.*1566GT[10]	NM_002538.4:c.*1566GT[11]	NM_002538.4:c.*1566GT[13]	NM_002538.4:c.*1566GT[14]	NM_002538.4:c.*1566GT[15]	NM_002538.4:c.*1566GT[16]	NM_002538.4:c.*1566GT[17]
OCLN transcript variant 1	NM_002538.3:c.1566_1589=	NM_002538.3:c.*1566GT[6]	NM_002538.3:c.*1566GT[7]	NM_002538.3:c.*1566GT[8]	NM_002538.3:c.*1566GT[9]	NM_002538.3:c.*1566GT[10]	NM_002538.3:c.*1566GT[11]	NM_002538.3:c.*1566GT[13]	NM_002538.3:c.*1566GT[14]	NM_002538.3:c.*1566GT[15]	NM_002538.3:c.*1566GT[16]	NM_002538.3:c.*1566GT[17]
OCLN transcript variant 2	NM_001205254.2:c.1566_1589=	NM_001205254.2:c.*1566GT[6]	NM_001205254.2:c.*1566GT[7]	NM_001205254.2:c.*1566GT[8]	NM_001205254.2:c.*1566GT[9]	NM_001205254.2:c.*1566GT[10]	NM_001205254.2:c.*1566GT[11]	NM_001205254.2:c.*1566GT[13]	NM_001205254.2:c.*1566GT[14]	NM_001205254.2:c.*1566GT[15]	NM_001205254.2:c.*1566GT[16]	NM_001205254.2:c.*1566GT[17]
OCLN transcript variant 2	NM_001205254.1:c.1566_1589=	NM_001205254.1:c.*1566GT[6]	NM_001205254.1:c.*1566GT[7]	NM_001205254.1:c.*1566GT[8]	NM_001205254.1:c.*1566GT[9]	NM_001205254.1:c.*1566GT[10]	NM_001205254.1:c.*1566GT[11]	NM_001205254.1:c.*1566GT[13]	NM_001205254.1:c.*1566GT[14]	NM_001205254.1:c.*1566GT[15]	NM_001205254.1:c.*1566GT[16]	NM_001205254.1:c.*1566GT[17]
OCLN transcript variant 3	NM_001205255.1:c.1566_1589=	NM_001205255.1:c.*1566GT[6]	NM_001205255.1:c.*1566GT[7]	NM_001205255.1:c.*1566GT[8]	NM_001205255.1:c.*1566GT[9]	NM_001205255.1:c.*1566GT[10]	NM_001205255.1:c.*1566GT[11]	NM_001205255.1:c.*1566GT[13]	NM_001205255.1:c.*1566GT[14]	NM_001205255.1:c.*1566GT[15]	NM_001205255.1:c.*1566GT[16]	NM_001205255.1:c.*1566GT[17]
GRCh38.p14 chr 5 alt locus HSCHR5_2_CTG1_1	NW_003315917.2:g.338180_338203=	NW_003315917.2:g.338180GT[6]	NW_003315917.2:g.338180GT[7]	NW_003315917.2:g.338180GT[8]	NW_003315917.2:g.338180GT[9]	NW_003315917.2:g.338180GT[10]	NW_003315917.2:g.338180GT[11]	NW_003315917.2:g.338180GT[13]	NW_003315917.2:g.338180GT[14]	NW_003315917.2:g.338180GT[15]	NW_003315917.2:g.338180GT[16]	NW_003315917.2:g.338180GT[17]
GRCh38.p14 chr 5 fix patch HG2405_PATCH	NW_025791777.1:g.221953GT[12]	NW_025791777.1:g.221953GT[6]	NW_025791777.1:g.221953GT[7]	NW_025791777.1:g.221953GT[8]	NW_025791777.1:g.221953GT[9]	NW_025791777.1:g.221953GT[10]	NW_025791777.1:g.221953_221974=	NW_025791777.1:g.221953GT[13]	NW_025791777.1:g.221953GT[14]	NW_025791777.1:g.221953GT[15]	NW_025791777.1:g.221953GT[16]	NW_025791777.1:g.221953GT[17]
OCLN transcript variant X4	XM_017008914.3:c.1566_1589=	XM_017008914.3:c.*1566GT[6]	XM_017008914.3:c.*1566GT[7]	XM_017008914.3:c.*1566GT[8]	XM_017008914.3:c.*1566GT[9]	XM_017008914.3:c.*1566GT[10]	XM_017008914.3:c.*1566GT[11]	XM_017008914.3:c.*1566GT[13]	XM_017008914.3:c.*1566GT[14]	XM_017008914.3:c.*1566GT[15]	XM_017008914.3:c.*1566GT[16]	XM_017008914.3:c.*1566GT[17]
OCLN transcript variant X3	XM_017008913.3:c.1566_1589=	XM_017008913.3:c.*1566GT[6]	XM_017008913.3:c.*1566GT[7]	XM_017008913.3:c.*1566GT[8]	XM_017008913.3:c.*1566GT[9]	XM_017008913.3:c.*1566GT[10]	XM_017008913.3:c.*1566GT[11]	XM_017008913.3:c.*1566GT[13]	XM_017008913.3:c.*1566GT[14]	XM_017008913.3:c.*1566GT[15]	XM_017008913.3:c.*1566GT[16]	XM_017008913.3:c.*1566GT[17]
OCLN transcript variant X1	XM_017008913.1:c.1566_1589=	XM_017008913.1:c.*1566GT[6]	XM_017008913.1:c.*1566GT[7]	XM_017008913.1:c.*1566GT[8]	XM_017008913.1:c.*1566GT[9]	XM_017008913.1:c.*1566GT[10]	XM_017008913.1:c.*1566GT[11]	XM_017008913.1:c.*1566GT[13]	XM_017008913.1:c.*1566GT[14]	XM_017008913.1:c.*1566GT[15]	XM_017008913.1:c.*1566GT[16]	XM_017008913.1:c.*1566GT[17]
OCLN transcript variant X2	XM_047416594.1:c.1566_1589=	XM_047416594.1:c.*1566GT[6]	XM_047416594.1:c.*1566GT[7]	XM_047416594.1:c.*1566GT[8]	XM_047416594.1:c.*1566GT[9]	XM_047416594.1:c.*1566GT[10]	XM_047416594.1:c.*1566GT[11]	XM_047416594.1:c.*1566GT[13]	XM_047416594.1:c.*1566GT[14]	XM_047416594.1:c.*1566GT[15]	XM_047416594.1:c.*1566GT[16]	XM_047416594.1:c.*1566GT[17]
OCLN transcript variant X1	XM_047416593.1:c.1566_1589=	XM_047416593.1:c.*1566GT[6]	XM_047416593.1:c.*1566GT[7]	XM_047416593.1:c.*1566GT[8]	XM_047416593.1:c.*1566GT[9]	XM_047416593.1:c.*1566GT[10]	XM_047416593.1:c.*1566GT[11]	XM_047416593.1:c.*1566GT[13]	XM_047416593.1:c.*1566GT[14]	XM_047416593.1:c.*1566GT[15]	XM_047416593.1:c.*1566GT[16]	XM_047416593.1:c.*1566GT[17]
OCLN transcript variant 4	NM_001410743.1:c.1566_1589=	NM_001410743.1:c.*1566GT[6]	NM_001410743.1:c.*1566GT[7]	NM_001410743.1:c.*1566GT[8]	NM_001410743.1:c.*1566GT[9]	NM_001410743.1:c.*1566GT[10]	NM_001410743.1:c.*1566GT[11]	NM_001410743.1:c.*1566GT[13]	NM_001410743.1:c.*1566GT[14]	NM_001410743.1:c.*1566GT[15]	NM_001410743.1:c.*1566GT[16]	NM_001410743.1:c.*1566GT[17]

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	LUNTER	ss551664030	Apr 25, 2013 (138)
2	BILGI_BIOE	ss666313761	Apr 25, 2013 (138)
3	SWEGEN	ss2997095798	Nov 08, 2017 (151)
4	MCHAISSO	ss3064160560	Nov 08, 2017 (151)
5	MCHAISSO	ss3066022392	Nov 08, 2017 (151)
6	URBANLAB	ss3648082688	Oct 12, 2018 (152)
7	ACPOP	ss3732443112	Jul 13, 2019 (153)
8	EVA	ss3838120290	Apr 26, 2020 (154)
9	EVA	ss3843561249	Apr 26, 2020 (154)
10	KOGIC	ss3956870661	Apr 26, 2020 (154)
11	KOGIC	ss3956870662	Apr 26, 2020 (154)
12	KOGIC	ss3956870663	Apr 26, 2020 (154)
13	KOGIC	ss3956870664	Apr 26, 2020 (154)
14	GNOMAD	ss4106235823	Apr 26, 2021 (155)
15	GNOMAD	ss4106235824	Apr 26, 2021 (155)
16	GNOMAD	ss4106235825	Apr 26, 2021 (155)
17	GNOMAD	ss4106235826	Apr 26, 2021 (155)
18	GNOMAD	ss4106235828	Apr 26, 2021 (155)
19	GNOMAD	ss4106235829	Apr 26, 2021 (155)
20	GNOMAD	ss4106235830	Apr 26, 2021 (155)
21	GNOMAD	ss4106235831	Apr 26, 2021 (155)
22	GNOMAD	ss4106235832	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5172194057	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5172194058	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5172194059	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5172194060	Apr 26, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5264325692	Oct 13, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5264325693	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5264325694	Oct 13, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5264325695	Oct 13, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5264325696	Oct 13, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5264325697	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5462469444	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5462469445	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5708719586	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5708719587	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5708719588	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5708719589	Oct 13, 2022 (156)
39	YY_MCH	ss5806405283	Oct 13, 2022 (156)
40	EVA	ss5854852776	Oct 13, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 191618128 (NC_000005.10:69555236::GT 4561/92370) Row 191618129 (NC_000005.10:69555236::GTGT 90/92372) Row 191618130 (NC_000005.10:69555236::GTGTGT 1/92370)...	-	Apr 26, 2021 (155)
50	Korean Genome Project Submission ignored due to conflicting rows: Row 13248662 (NC_000005.10:69555240::GT 5/870) Row 13248663 (NC_000005.10:69555238:GT: 14/870) Row 13248664 (NC_000005.10:69555240::GTGT 6/870)...	-	Apr 26, 2020 (154)
51	Korean Genome Project Submission ignored due to conflicting rows: Row 13248662 (NC_000005.10:69555240::GT 5/870) Row 13248663 (NC_000005.10:69555238:GT: 14/870) Row 13248664 (NC_000005.10:69555240::GTGT 6/870)...	-	Apr 26, 2020 (154)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 13248662 (NC_000005.10:69555240::GT 5/870) Row 13248663 (NC_000005.10:69555238:GT: 14/870) Row 13248664 (NC_000005.10:69555240::GTGT 6/870)...	-	Apr 26, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 13248662 (NC_000005.10:69555240::GT 5/870) Row 13248663 (NC_000005.10:69555238:GT: 14/870) Row 13248664 (NC_000005.10:69555240::GTGT 6/870)...	-	Apr 26, 2020 (154)
54	Northern Sweden	NC_000005.9 - 68851064	Jul 13, 2019 (153)
55	8.3KJPN Submission ignored due to conflicting rows: Row 30163364 (NC_000005.9:68851063:GT: 9567/16582) Row 30163365 (NC_000005.9:68851063::GT 16/16582) Row 30163366 (NC_000005.9:68851063::GTGT 6/16582)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 30163364 (NC_000005.9:68851063:GT: 9567/16582) Row 30163365 (NC_000005.9:68851063::GT 16/16582) Row 30163366 (NC_000005.9:68851063::GTGT 6/16582)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 30163364 (NC_000005.9:68851063:GT: 9567/16582) Row 30163365 (NC_000005.9:68851063::GT 16/16582) Row 30163366 (NC_000005.9:68851063::GTGT 6/16582)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 30163364 (NC_000005.9:68851063:GT: 9567/16582) Row 30163365 (NC_000005.9:68851063::GT 16/16582) Row 30163366 (NC_000005.9:68851063::GTGT 6/16582)...	-	Apr 26, 2021 (155)
59	14KJPN Submission ignored due to conflicting rows: Row 42556690 (NC_000005.10:69555236:GT: 14234/27268) Row 42556691 (NC_000005.10:69555236::GT 32/27268) Row 42556692 (NC_000005.10:69555236::GTGT 8/27268)...	-	Oct 13, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 42556690 (NC_000005.10:69555236:GT: 14234/27268) Row 42556691 (NC_000005.10:69555236::GT 32/27268) Row 42556692 (NC_000005.10:69555236::GTGT 8/27268)...	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 42556690 (NC_000005.10:69555236:GT: 14234/27268) Row 42556691 (NC_000005.10:69555236::GT 32/27268) Row 42556692 (NC_000005.10:69555236::GTGT 8/27268)...	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 42556690 (NC_000005.10:69555236:GT: 14234/27268) Row 42556691 (NC_000005.10:69555236::GT 32/27268) Row 42556692 (NC_000005.10:69555236::GTGT 8/27268)...	-	Oct 13, 2022 (156)
63	ALFA	NC_000005.10 - 69555237	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4106235832	NC_000005.10:69555236:GTGTGTGTGTGT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
ss4106235831	NC_000005.10:69555236:GTGTGTGTGT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
ss4106235830, ss5264325697	NC_000005.10:69555236:GTGTGTGT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	(self)
ss4106235829, ss5264325696	NC_000005.10:69555236:GTGTGT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
ss2997095798, ss5172194060	NC_000005.9:68851063:GTGT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
ss3956870664, ss4106235828, ss5264325695, ss5708719589	NC_000005.10:69555236:GTGT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
ss551664030	NC_000005.8:68886819:GT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
5727977, ss666313761, ss3732443112, ss3838120290, ss5172194057	NC_000005.9:68851063:GT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064160560, ss3066022392, ss3648082688, ss3843561249, ss5264325692, ss5462469444, ss5708719586, ss5806405283, ss5854852776	NC_000005.10:69555236:GT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss3956870662	NC_000005.10:69555238:GT:	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss5172194058	NC_000005.9:68851063::GT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4106235823, ss5264325693, ss5462469445, ss5708719587	NC_000005.10:69555236::GT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3956870661	NC_000005.10:69555240::GT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5172194059	NC_000005.9:68851063::GTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4106235824, ss5264325694, ss5708719588	NC_000005.10:69555236::GTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3956870663	NC_000005.10:69555240::GTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4106235825	NC_000005.10:69555236::GTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4106235826	NC_000005.10:69555236::GTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1230829168	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:69555236:GTGTGTGTGTGT… NC_000005.10:69555236:GTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)

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

No publications for rs373178468

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

Genome context:

Select flank length:

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

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs373178468