Name: rs58692527
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.

rs58692527

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:178062864-178062886 (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(GA)₅ / del(GA)₄ / del(GA)₃ / d…
del(GA)₅ / del(GA)₄ / del(GA)₃ / delGAGA / delGA / dupGA / dupGAGA / dup(GA)₃ / dup(GA)₄ / dup(GA)₅ / dup(GA)₆ / dup(GA)₇ / dup(GA)₈ / dup(GA)₉
Variation Type: Indel Insertion and Deletion
Frequency: (AG)₁₁A=0.2624 (1263/4814, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM153CP : 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	4814	AGAGAGAGAGAGAGAGAGAGAGA=0.2624	AGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGA=0.3614, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.1263, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.2235, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0093, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0162, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0008, AGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000	0.274949	0.336049	0.389002	25
European	Sub	4752	AGAGAGAGAGAGAGAGAGAGAGA=0.2538	AGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGA=0.3655, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.1277, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.2264, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0095, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0164, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0006, AGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0000	0.254202	0.345588	0.40021	19
African	Sub	12	AGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AGAGAGAGAGAGAGAGAGAGAGA=0	AGAGAGAGAGAGA=0, AGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	0	0	0	N/A
African American	Sub	12	AGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	8	AGAGAGAGAGAGAGAGAGAGAGA=1.0	AGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	0	AGAGAGAGAGAGAGAGAGAGAGA=0	AGAGAGAGAGAGA=0, AGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	0	0	0	N/A
Other Asian	Sub	8	AGAGAGAGAGAGAGAGAGAGAGA=1.0	AGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	6	AGAGAGAGAGAGAGAGAGAGAGA=1.0	AGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	12	AGAGAGAGAGAGAGAGAGAGAGA=1.00	AGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	AGAGAGAGAGAGAGAGAGAGAGA=0	AGAGAGAGAGAGA=0, AGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0	0	0	0	N/A
Other	Sub	24	AGAGAGAGAGAGAGAGAGAGAGA=0.79	AGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGA=0.12, AGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.04, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGA=0.04, AGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00, AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA=0.00	0.818182	0.090909	0.090909	3

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	4814	(AG)₁₁A=0.2624	del(GA)₅=0.0000, del(GA)₄=0.0000, del(GA)₃=0.3614, delGAGA=0.0000, delGA=0.0000, dupGA=0.0162, dupGAGA=0.0008, dup(GA)₃=0.1263, dup(GA)₄=0.2235, dup(GA)₅=0.0093, dup(GA)₆=0.0000, dup(GA)₇=0.0000, dup(GA)₈=0.0000, dup(GA)₉=0.0000
Allele Frequency Aggregator	European	Sub	4752	(AG)₁₁A=0.2538	del(GA)₅=0.0000, del(GA)₄=0.0000, del(GA)₃=0.3655, delGAGA=0.0000, delGA=0.0000, dupGA=0.0164, dupGAGA=0.0006, dup(GA)₃=0.1277, dup(GA)₄=0.2264, dup(GA)₅=0.0095, dup(GA)₆=0.0000, dup(GA)₇=0.0000, dup(GA)₈=0.0000, dup(GA)₉=0.0000
Allele Frequency Aggregator	Other	Sub	24	(AG)₁₁A=0.79	del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.12, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.04, dup(GA)₃=0.04, dup(GA)₄=0.00, dup(GA)₅=0.00, dup(GA)₆=0.00, dup(GA)₇=0.00, dup(GA)₈=0.00, dup(GA)₉=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(AG)₁₁A=1.00	del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00, dup(GA)₆=0.00, dup(GA)₇=0.00, dup(GA)₈=0.00, dup(GA)₉=0.00
Allele Frequency Aggregator	African	Sub	12	(AG)₁₁A=1.00	del(GA)₅=0.00, del(GA)₄=0.00, del(GA)₃=0.00, delGAGA=0.00, delGA=0.00, dupGA=0.00, dupGAGA=0.00, dup(GA)₃=0.00, dup(GA)₄=0.00, dup(GA)₅=0.00, dup(GA)₆=0.00, dup(GA)₇=0.00, dup(GA)₈=0.00, dup(GA)₉=0.00
Allele Frequency Aggregator	Asian	Sub	8	(AG)₁₁A=1.0	del(GA)₅=0.0, del(GA)₄=0.0, del(GA)₃=0.0, delGAGA=0.0, delGA=0.0, dupGA=0.0, dupGAGA=0.0, dup(GA)₃=0.0, dup(GA)₄=0.0, dup(GA)₅=0.0, dup(GA)₆=0.0, dup(GA)₇=0.0, dup(GA)₈=0.0, dup(GA)₉=0.0
Allele Frequency Aggregator	Latin American 1	Sub	6	(AG)₁₁A=1.0	del(GA)₅=0.0, del(GA)₄=0.0, del(GA)₃=0.0, delGAGA=0.0, delGA=0.0, dupGA=0.0, dupGAGA=0.0, dup(GA)₃=0.0, dup(GA)₄=0.0, dup(GA)₅=0.0, dup(GA)₆=0.0, dup(GA)₇=0.0, dup(GA)₈=0.0, dup(GA)₉=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(AG)₁₁A=0	del(GA)₅=0, del(GA)₄=0, del(GA)₃=0, delGAGA=0, delGA=0, dupGA=0, dupGAGA=0, dup(GA)₃=0, dup(GA)₄=0, dup(GA)₅=0, dup(GA)₆=0, dup(GA)₇=0, dup(GA)₈=0, dup(GA)₉=0

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.178062865GA[6]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[7]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[8]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[9]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[10]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[12]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[13]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[14]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[15]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[16]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[17]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[18]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[19]
GRCh38.p14 chr 5	NC_000005.10:g.178062865GA[20]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[6]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[7]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[8]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[9]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[10]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[12]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[13]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[14]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[15]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[16]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[17]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[18]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[19]
GRCh37.p13 chr 5	NC_000005.9:g.177489866GA[20]

Gene: FAM153CP, family with sequence similarity 153 member C, pseudogene (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM153CP transcript variant 2	NR_149722.1:n.	N/A	Intron Variant
FAM153CP transcript variant 1	NR_159407.1:n.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(AG)₁₁A=	del(GA)₅	del(GA)₄	del(GA)₃	delGAGA	delGA	dupGA	dupGAGA	dup(GA)₃	dup(GA)₄	dup(GA)₅	dup(GA)₆	dup(GA)₇	dup(GA)₈	dup(GA)₉
GRCh38.p14 chr 5	NC_000005.10:g.178062864_178062886=	NC_000005.10:g.178062865GA[6]	NC_000005.10:g.178062865GA[7]	NC_000005.10:g.178062865GA[8]	NC_000005.10:g.178062865GA[9]	NC_000005.10:g.178062865GA[10]	NC_000005.10:g.178062865GA[12]	NC_000005.10:g.178062865GA[13]	NC_000005.10:g.178062865GA[14]	NC_000005.10:g.178062865GA[15]	NC_000005.10:g.178062865GA[16]	NC_000005.10:g.178062865GA[17]	NC_000005.10:g.178062865GA[18]	NC_000005.10:g.178062865GA[19]	NC_000005.10:g.178062865GA[20]
GRCh37.p13 chr 5	NC_000005.9:g.177489865_177489887=	NC_000005.9:g.177489866GA[6]	NC_000005.9:g.177489866GA[7]	NC_000005.9:g.177489866GA[8]	NC_000005.9:g.177489866GA[9]	NC_000005.9:g.177489866GA[10]	NC_000005.9:g.177489866GA[12]	NC_000005.9:g.177489866GA[13]	NC_000005.9:g.177489866GA[14]	NC_000005.9:g.177489866GA[15]	NC_000005.9:g.177489866GA[16]	NC_000005.9:g.177489866GA[17]	NC_000005.9:g.177489866GA[18]	NC_000005.9:g.177489866GA[19]	NC_000005.9:g.177489866GA[20]

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#.

68 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82147186	Dec 04, 2013 (142)
2	HUMANGENOME_JCVI	ss95415611	Mar 15, 2016 (147)
3	HUMANGENOME_JCVI	ss98686175	Feb 13, 2009 (130)
4	BUSHMAN	ss193839083	Jul 04, 2010 (132)
5	GMI	ss288676679	May 04, 2012 (138)
6	GMI	ss288676680	May 04, 2012 (137)
7	1000GENOMES	ss326752835	May 09, 2011 (138)
8	1000GENOMES	ss326798341	May 09, 2011 (138)
9	1000GENOMES	ss327034156	May 09, 2011 (134)
10	LUNTER	ss551572091	Apr 25, 2013 (138)
11	LUNTER	ss551749047	Apr 25, 2013 (138)
12	LUNTER	ss553229417	Apr 25, 2013 (138)
13	TISHKOFF	ss554245470	Apr 25, 2013 (138)
14	SSMP	ss663586611	Apr 01, 2015 (144)
15	BILGI_BIOE	ss666338661	Apr 25, 2013 (138)
16	HAMMER_LAB	ss1804224107	Sep 08, 2015 (146)
17	SWEGEN	ss2998326143	Nov 08, 2017 (151)
18	MCHAISSO	ss3064187156	Nov 08, 2017 (151)
19	MCHAISSO	ss3065063355	Nov 08, 2017 (151)
20	MCHAISSO	ss3066058609	Nov 08, 2017 (151)
21	URBANLAB	ss3648239505	Oct 12, 2018 (152)
22	PACBIO	ss3785338680	Jul 13, 2019 (153)
23	PACBIO	ss3785338681	Jul 13, 2019 (153)
24	PACBIO	ss3790708097	Jul 13, 2019 (153)
25	PACBIO	ss3790708098	Jul 13, 2019 (153)
26	PACBIO	ss3795585263	Jul 13, 2019 (153)
27	PACBIO	ss3795585264	Jul 13, 2019 (153)
28	EVA	ss3838307886	Apr 26, 2020 (154)
29	GNOMAD	ss4135072721	Apr 26, 2021 (155)
30	GNOMAD	ss4135072723	Apr 26, 2021 (155)
31	GNOMAD	ss4135072724	Apr 26, 2021 (155)
32	GNOMAD	ss4135072725	Apr 26, 2021 (155)
33	GNOMAD	ss4135072726	Apr 26, 2021 (155)
34	GNOMAD	ss4135072727	Apr 26, 2021 (155)
35	GNOMAD	ss4135072728	Apr 26, 2021 (155)
36	GNOMAD	ss4135072729	Apr 26, 2021 (155)
37	GNOMAD	ss4135072730	Apr 26, 2021 (155)
38	GNOMAD	ss4135072735	Apr 26, 2021 (155)
39	GNOMAD	ss4135072736	Apr 26, 2021 (155)
40	GNOMAD	ss4135072737	Apr 26, 2021 (155)
41	GNOMAD	ss4135072738	Apr 26, 2021 (155)
42	GNOMAD	ss4135072739	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5175642907	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5175642908	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5175642909	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5175642910	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5175642911	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5175642912	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5266999738	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5266999739	Oct 13, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5266999740	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5266999741	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5464837608	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5464837609	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5464837610	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5464837611	Oct 13, 2022 (156)
57	HUGCELL_USP	ss5464837612	Oct 13, 2022 (156)
58	HUGCELL_USP	ss5464837613	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5713155025	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5713155026	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5713155027	Oct 13, 2022 (156)
62	TOMMO_GENOMICS	ss5713155028	Oct 13, 2022 (156)
63	TOMMO_GENOMICS	ss5713155029	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5713155030	Oct 13, 2022 (156)
65	EVA	ss5836092571	Oct 13, 2022 (156)
66	EVA	ss5836092572	Oct 13, 2022 (156)
67	EVA	ss5836092573	Oct 13, 2022 (156)
68	EVA	ss5897648842	Oct 13, 2022 (156)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213952906 (NC_000005.10:178062863::AG 5337/135850) Row 213952908 (NC_000005.10:178062863::AGAG 783/135844) Row 213952909 (NC_000005.10:178062863::AGAGAG 24111/135570)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 33612214 (NC_000005.9:177489864:AGAGAG: 7817/16760) Row 33612215 (NC_000005.9:177489864::AGAGAG 1489/16760) Row 33612216 (NC_000005.9:177489864::AGAG 29/16760)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 33612214 (NC_000005.9:177489864:AGAGAG: 7817/16760) Row 33612215 (NC_000005.9:177489864::AGAGAG 1489/16760) Row 33612216 (NC_000005.9:177489864::AGAG 29/16760)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 33612214 (NC_000005.9:177489864:AGAGAG: 7817/16760) Row 33612215 (NC_000005.9:177489864::AGAGAG 1489/16760) Row 33612216 (NC_000005.9:177489864::AGAG 29/16760)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 33612214 (NC_000005.9:177489864:AGAGAG: 7817/16760) Row 33612215 (NC_000005.9:177489864::AGAGAG 1489/16760) Row 33612216 (NC_000005.9:177489864::AGAG 29/16760)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 33612214 (NC_000005.9:177489864:AGAGAG: 7817/16760) Row 33612215 (NC_000005.9:177489864::AGAGAG 1489/16760) Row 33612216 (NC_000005.9:177489864::AGAG 29/16760)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 33612214 (NC_000005.9:177489864:AGAGAG: 7817/16760) Row 33612215 (NC_000005.9:177489864::AGAGAG 1489/16760) Row 33612216 (NC_000005.9:177489864::AGAG 29/16760)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 46992129 (NC_000005.10:178062863:AGAGAG: 13029/28080) Row 46992130 (NC_000005.10:178062863::AGAGAGAG 3818/28080) Row 46992131 (NC_000005.10:178062863::AGAGAG 2222/28080)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 46992129 (NC_000005.10:178062863:AGAGAG: 13029/28080) Row 46992130 (NC_000005.10:178062863::AGAGAGAG 3818/28080) Row 46992131 (NC_000005.10:178062863::AGAGAG 2222/28080)...	-	Oct 13, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 46992129 (NC_000005.10:178062863:AGAGAG: 13029/28080) Row 46992130 (NC_000005.10:178062863::AGAGAGAG 3818/28080) Row 46992131 (NC_000005.10:178062863::AGAGAG 2222/28080)...	-	Oct 13, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 46992129 (NC_000005.10:178062863:AGAGAG: 13029/28080) Row 46992130 (NC_000005.10:178062863::AGAGAGAG 3818/28080) Row 46992131 (NC_000005.10:178062863::AGAGAG 2222/28080)...	-	Oct 13, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 46992129 (NC_000005.10:178062863:AGAGAG: 13029/28080) Row 46992130 (NC_000005.10:178062863::AGAGAGAG 3818/28080) Row 46992131 (NC_000005.10:178062863::AGAGAG 2222/28080)...	-	Oct 13, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 46992129 (NC_000005.10:178062863:AGAGAG: 13029/28080) Row 46992130 (NC_000005.10:178062863::AGAGAGAG 3818/28080) Row 46992131 (NC_000005.10:178062863::AGAGAG 2222/28080)...	-	Oct 13, 2022 (156)
95	ALFA	NC_000005.10 - 178062864	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)
rs137998472	Apr 25, 2013 (138)
rs397964011	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4135072739	NC_000005.10:178062863:AGAGAGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGA	(self)
ss4135072738	NC_000005.10:178062863:AGAGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA	(self)
ss288676679, ss326752835, ss326798341, ss551572091, ss553229417	NC_000005.8:177422470:AGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss663586611, ss1804224107, ss2998326143, ss3785338680, ss3790708097, ss3795585263, ss3838307886, ss5175642907, ss5836092571	NC_000005.9:177489864:AGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss554245470	NC_000005.9:177489881:GAGAGA:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss3064187156, ss3648239505, ss4135072737, ss5266999738, ss5464837610, ss5713155025, ss5897648842	NC_000005.10:178062863:AGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss98686175	NT_023133.13:22301137:AGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss95415611	NT_023133.13:22301154:GAGAGA:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss193839083	NT_023133.14:22301539:AGAGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA	(self)
ss4135072736	NC_000005.10:178062863:AGAG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA	(self)
ss4135072735	NC_000005.10:178062863:AG:	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA	(self)
ss3785338681, ss3790708098, ss3795585264, ss5175642912	NC_000005.9:177489864::AG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072721, ss5266999741, ss5464837611, ss5713155030	NC_000005.10:178062863::AG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss5175642909	NC_000005.9:177489864::AGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072723, ss5464837613, ss5713155029	NC_000005.10:178062863::AGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss288676680	NC_000005.8:177422493::GAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss5175642908, ss5836092572	NC_000005.9:177489864::AGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss3065063355, ss3066058609, ss4135072724, ss5266999740, ss5464837608, ss5713155027	NC_000005.10:178062863::AGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss327034156, ss551749047	NC_000005.8:177422470::AGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss666338661, ss5175642910, ss5836092573	NC_000005.9:177489864::AGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072725, ss5266999739, ss5464837609, ss5713155026	NC_000005.10:178062863::AGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss82147186	NT_023133.13:22301160::GAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss5175642911	NC_000005.9:177489864::AGAGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072726, ss5464837612, ss5713155028	NC_000005.10:178062863::AGAGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072727	NC_000005.10:178062863::AGAGAGAGAG… NC_000005.10:178062863::AGAGAGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072728	NC_000005.10:178062863::AGAGAGAGAG… NC_000005.10:178062863::AGAGAGAGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072729	NC_000005.10:178062863::AGAGAGAGAG… NC_000005.10:178062863::AGAGAGAGAGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
ss4135072730	NC_000005.10:178062863::AGAGAGAGAG… NC_000005.10:178062863::AGAGAGAGAGAGAGAGAG	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(self)
3357018230	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	NC_000005.10:178062863:AGAGAGAGAGA… NC_000005.10:178062863:AGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA	(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 rs58692527

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

rs58692527