Name: rs55949628
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.

rs55949628

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:38381947-38381974 (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(A)₁₇ / del(A)₁₅ / del(A)₁₄ / d…
del(A)₁₇ / del(A)₁₅ / del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆ / dup(A)₈ / dup(A)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.000404 (107/264690, TOPMED)
del(A)₁₇=0.0000 (0/9872, ALFA)
del(A)₁₅=0.0000 (0/9872, ALFA) (+ 18 more)
del(A)₁₄=0.0000 (0/9872, ALFA)
del(A)₁₃=0.0000 (0/9872, ALFA)
del(A)₁₂=0.0000 (0/9872, ALFA)
del(A)₁₁=0.0000 (0/9872, ALFA)
del(A)₁₀=0.0000 (0/9872, ALFA)
del(A)₉=0.0000 (0/9872, ALFA)
del(A)₈=0.0000 (0/9872, ALFA)
del(A)₇=0.0000 (0/9872, ALFA)
del(A)₆=0.0000 (0/9872, ALFA)
del(A)₅=0.0000 (0/9872, ALFA)
del(A)₄=0.0000 (0/9872, ALFA)
delAAA=0.0000 (0/9872, ALFA)
delAA=0.0000 (0/9872, ALFA)
delA=0.0000 (0/9872, ALFA)
dupA=0.0000 (0/9872, ALFA)
dupAA=0.0000 (0/9872, ALFA)
dupAAA=0.0000 (0/9872, ALFA)
dup(A)₄=0.0000 (0/9872, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SOCS7 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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
TopMed	Global	Study-wide	264690	(A)₂₈=0.999596	del(A)₁₃=0.000404
Allele Frequency Aggregator	Total	Global	9872	(A)₂₈=1.0000	del(A)₁₇=0.0000, del(A)₁₅=0.0000, del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	6958	(A)₂₈=1.0000	del(A)₁₇=0.0000, del(A)₁₅=0.0000, del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	1718	(A)₂₈=1.0000	del(A)₁₇=0.0000, del(A)₁₅=0.0000, del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	558	(A)₂₈=1.000	del(A)₁₇=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	390	(A)₂₈=1.000	del(A)₁₇=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	118	(A)₂₈=1.000	del(A)₁₇=0.000, del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	74	(A)₂₈=1.00	del(A)₁₇=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	56	(A)₂₈=1.00	del(A)₁₇=0.00, del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 17	NC_000017.11:g.38381958_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381960_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381961_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381962_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381963_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381964_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381965_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381966_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381967_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381968_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381969_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381970_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381971_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381972_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381973_38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381974del
GRCh38.p14 chr 17	NC_000017.11:g.38381974dup
GRCh38.p14 chr 17	NC_000017.11:g.38381973_38381974dup
GRCh38.p14 chr 17	NC_000017.11:g.38381972_38381974dup
GRCh38.p14 chr 17	NC_000017.11:g.38381971_38381974dup
GRCh38.p14 chr 17	NC_000017.11:g.38381969_38381974dup
GRCh38.p14 chr 17	NC_000017.11:g.38381967_38381974dup
GRCh38.p14 chr 17	NC_000017.11:g.38381964_38381974dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165169_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165171_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165172_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165173_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165174_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165175_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165176_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165177_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165178_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165179_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165180_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165181_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165182_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165183_165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165184del
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165183_165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165182_165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165181_165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165180_165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165178_165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165176_165184dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165173_165184dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416850_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416852_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416853_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416854_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416855_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416856_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416857_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416858_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416859_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416860_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416861_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416862_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416863_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416864_2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416865del
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416864_2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416863_2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416862_2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416861_2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416859_2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416857_2416865dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416854_2416865dup
GRCh37.p13 chr 17	NC_000017.10:g.36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537784_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537786_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537787_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537788_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537789_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537790_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537791_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537792_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537793_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537794_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537795_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537796_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537797_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537798_36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537799del
GRCh37.p13 chr 17	NC_000017.10:g.36537798_36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537797_36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537796_36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537795_36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537793_36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537791_36537799dup
GRCh37.p13 chr 17	NC_000017.10:g.36537788_36537799dup

Gene: SOCS7, suppressor of cytokine signaling 7 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SOCS7 transcript	NM_014598.4:c.1681+4116_1… NM_014598.4:c.1681+4116_1681+4132del	N/A	Intron Variant
SOCS7 transcript variant X1	XM_017024551.2:c.1579+411… XM_017024551.2:c.1579+4116_1579+4132del	N/A	Intron Variant
SOCS7 transcript variant X2	XM_017024552.2:c.1474+411… XM_017024552.2:c.1474+4116_1474+4132del	N/A	Intron Variant
SOCS7 transcript variant X3	XR_007065295.1: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	(A)₂₈=	del(A)₁₇	del(A)₁₅	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆	dup(A)₈	dup(A)₁₁
GRCh38.p14 chr 17	NC_000017.11:g.38381947_38381974=	NC_000017.11:g.38381958_38381974del	NC_000017.11:g.38381960_38381974del	NC_000017.11:g.38381961_38381974del	NC_000017.11:g.38381962_38381974del	NC_000017.11:g.38381963_38381974del	NC_000017.11:g.38381964_38381974del	NC_000017.11:g.38381965_38381974del	NC_000017.11:g.38381966_38381974del	NC_000017.11:g.38381967_38381974del	NC_000017.11:g.38381968_38381974del	NC_000017.11:g.38381969_38381974del	NC_000017.11:g.38381970_38381974del	NC_000017.11:g.38381971_38381974del	NC_000017.11:g.38381972_38381974del	NC_000017.11:g.38381973_38381974del	NC_000017.11:g.38381974del	NC_000017.11:g.38381974dup	NC_000017.11:g.38381973_38381974dup	NC_000017.11:g.38381972_38381974dup	NC_000017.11:g.38381971_38381974dup	NC_000017.11:g.38381969_38381974dup	NC_000017.11:g.38381967_38381974dup	NC_000017.11:g.38381964_38381974dup
GRCh37.p13 chr 17 fix patch HG745_PATCH	NW_003315948.2:g.165184dup	NW_003315948.2:g.165169_165184del	NW_003315948.2:g.165171_165184del	NW_003315948.2:g.165172_165184del	NW_003315948.2:g.165173_165184del	NW_003315948.2:g.165174_165184del	NW_003315948.2:g.165175_165184del	NW_003315948.2:g.165176_165184del	NW_003315948.2:g.165177_165184del	NW_003315948.2:g.165178_165184del	NW_003315948.2:g.165179_165184del	NW_003315948.2:g.165180_165184del	NW_003315948.2:g.165181_165184del	NW_003315948.2:g.165182_165184del	NW_003315948.2:g.165183_165184del	NW_003315948.2:g.165184del	NW_003315948.2:g.165158_165184=	NW_003315948.2:g.165183_165184dup	NW_003315948.2:g.165182_165184dup	NW_003315948.2:g.165181_165184dup	NW_003315948.2:g.165180_165184dup	NW_003315948.2:g.165178_165184dup	NW_003315948.2:g.165176_165184dup	NW_003315948.2:g.165173_165184dup
GRCh38.p14 chr 17 alt locus HSCHR17_7_CTG4	NT_187614.1:g.2416865dup	NT_187614.1:g.2416850_2416865del	NT_187614.1:g.2416852_2416865del	NT_187614.1:g.2416853_2416865del	NT_187614.1:g.2416854_2416865del	NT_187614.1:g.2416855_2416865del	NT_187614.1:g.2416856_2416865del	NT_187614.1:g.2416857_2416865del	NT_187614.1:g.2416858_2416865del	NT_187614.1:g.2416859_2416865del	NT_187614.1:g.2416860_2416865del	NT_187614.1:g.2416861_2416865del	NT_187614.1:g.2416862_2416865del	NT_187614.1:g.2416863_2416865del	NT_187614.1:g.2416864_2416865del	NT_187614.1:g.2416865del	NT_187614.1:g.2416839_2416865=	NT_187614.1:g.2416864_2416865dup	NT_187614.1:g.2416863_2416865dup	NT_187614.1:g.2416862_2416865dup	NT_187614.1:g.2416861_2416865dup	NT_187614.1:g.2416859_2416865dup	NT_187614.1:g.2416857_2416865dup	NT_187614.1:g.2416854_2416865dup
GRCh37.p13 chr 17	NC_000017.10:g.36537799dup	NC_000017.10:g.36537784_36537799del	NC_000017.10:g.36537786_36537799del	NC_000017.10:g.36537787_36537799del	NC_000017.10:g.36537788_36537799del	NC_000017.10:g.36537789_36537799del	NC_000017.10:g.36537790_36537799del	NC_000017.10:g.36537791_36537799del	NC_000017.10:g.36537792_36537799del	NC_000017.10:g.36537793_36537799del	NC_000017.10:g.36537794_36537799del	NC_000017.10:g.36537795_36537799del	NC_000017.10:g.36537796_36537799del	NC_000017.10:g.36537797_36537799del	NC_000017.10:g.36537798_36537799del	NC_000017.10:g.36537799del	NC_000017.10:g.36537773_36537799=	NC_000017.10:g.36537798_36537799dup	NC_000017.10:g.36537797_36537799dup	NC_000017.10:g.36537796_36537799dup	NC_000017.10:g.36537795_36537799dup	NC_000017.10:g.36537793_36537799dup	NC_000017.10:g.36537791_36537799dup	NC_000017.10:g.36537788_36537799dup
SOCS7 transcript	NM_014598.2:c.1489+4131dup	NM_014598.2:c.1489+4116_1489+4131del	NM_014598.2:c.1489+4118_1489+4131del	NM_014598.2:c.1489+4119_1489+4131del	NM_014598.2:c.1489+4120_1489+4131del	NM_014598.2:c.1489+4121_1489+4131del	NM_014598.2:c.1489+4122_1489+4131del	NM_014598.2:c.1489+4123_1489+4131del	NM_014598.2:c.1489+4124_1489+4131del	NM_014598.2:c.1489+4125_1489+4131del	NM_014598.2:c.1489+4126_1489+4131del	NM_014598.2:c.1489+4127_1489+4131del	NM_014598.2:c.1489+4128_1489+4131del	NM_014598.2:c.1489+4129_1489+4131del	NM_014598.2:c.1489+4130_1489+4131del	NM_014598.2:c.1489+4131del	NM_014598.2:c.1489+4105=	NM_014598.2:c.1489+4130_1489+4131dup	NM_014598.2:c.1489+4129_1489+4131dup	NM_014598.2:c.1489+4128_1489+4131dup	NM_014598.2:c.1489+4127_1489+4131dup	NM_014598.2:c.1489+4125_1489+4131dup	NM_014598.2:c.1489+4123_1489+4131dup	NM_014598.2:c.1489+4120_1489+4131dup
SOCS7 transcript	NM_014598.4:c.1681+4105=	NM_014598.4:c.1681+4116_1681+4132del	NM_014598.4:c.1681+4118_1681+4132del	NM_014598.4:c.1681+4119_1681+4132del	NM_014598.4:c.1681+4120_1681+4132del	NM_014598.4:c.1681+4121_1681+4132del	NM_014598.4:c.1681+4122_1681+4132del	NM_014598.4:c.1681+4123_1681+4132del	NM_014598.4:c.1681+4124_1681+4132del	NM_014598.4:c.1681+4125_1681+4132del	NM_014598.4:c.1681+4126_1681+4132del	NM_014598.4:c.1681+4127_1681+4132del	NM_014598.4:c.1681+4128_1681+4132del	NM_014598.4:c.1681+4129_1681+4132del	NM_014598.4:c.1681+4130_1681+4132del	NM_014598.4:c.1681+4131_1681+4132del	NM_014598.4:c.1681+4132del	NM_014598.4:c.1681+4132dup	NM_014598.4:c.1681+4131_1681+4132dup	NM_014598.4:c.1681+4130_1681+4132dup	NM_014598.4:c.1681+4129_1681+4132dup	NM_014598.4:c.1681+4127_1681+4132dup	NM_014598.4:c.1681+4125_1681+4132dup	NM_014598.4:c.1681+4122_1681+4132dup
SOCS7 transcript variant X1	XM_005257264.1:c.1387+4131dup	XM_005257264.1:c.1387+4116_1387+4131del	XM_005257264.1:c.1387+4118_1387+4131del	XM_005257264.1:c.1387+4119_1387+4131del	XM_005257264.1:c.1387+4120_1387+4131del	XM_005257264.1:c.1387+4121_1387+4131del	XM_005257264.1:c.1387+4122_1387+4131del	XM_005257264.1:c.1387+4123_1387+4131del	XM_005257264.1:c.1387+4124_1387+4131del	XM_005257264.1:c.1387+4125_1387+4131del	XM_005257264.1:c.1387+4126_1387+4131del	XM_005257264.1:c.1387+4127_1387+4131del	XM_005257264.1:c.1387+4128_1387+4131del	XM_005257264.1:c.1387+4129_1387+4131del	XM_005257264.1:c.1387+4130_1387+4131del	XM_005257264.1:c.1387+4131del	XM_005257264.1:c.1387+4105=	XM_005257264.1:c.1387+4130_1387+4131dup	XM_005257264.1:c.1387+4129_1387+4131dup	XM_005257264.1:c.1387+4128_1387+4131dup	XM_005257264.1:c.1387+4127_1387+4131dup	XM_005257264.1:c.1387+4125_1387+4131dup	XM_005257264.1:c.1387+4123_1387+4131dup	XM_005257264.1:c.1387+4120_1387+4131dup
SOCS7 transcript variant X2	XM_005257265.1:c.1282+4131dup	XM_005257265.1:c.1282+4116_1282+4131del	XM_005257265.1:c.1282+4118_1282+4131del	XM_005257265.1:c.1282+4119_1282+4131del	XM_005257265.1:c.1282+4120_1282+4131del	XM_005257265.1:c.1282+4121_1282+4131del	XM_005257265.1:c.1282+4122_1282+4131del	XM_005257265.1:c.1282+4123_1282+4131del	XM_005257265.1:c.1282+4124_1282+4131del	XM_005257265.1:c.1282+4125_1282+4131del	XM_005257265.1:c.1282+4126_1282+4131del	XM_005257265.1:c.1282+4127_1282+4131del	XM_005257265.1:c.1282+4128_1282+4131del	XM_005257265.1:c.1282+4129_1282+4131del	XM_005257265.1:c.1282+4130_1282+4131del	XM_005257265.1:c.1282+4131del	XM_005257265.1:c.1282+4105=	XM_005257265.1:c.1282+4130_1282+4131dup	XM_005257265.1:c.1282+4129_1282+4131dup	XM_005257265.1:c.1282+4128_1282+4131dup	XM_005257265.1:c.1282+4127_1282+4131dup	XM_005257265.1:c.1282+4125_1282+4131dup	XM_005257265.1:c.1282+4123_1282+4131dup	XM_005257265.1:c.1282+4120_1282+4131dup
SOCS7 transcript variant X1	XM_005276891.1:c.1387+4131dup	XM_005276891.1:c.1387+4116_1387+4131del	XM_005276891.1:c.1387+4118_1387+4131del	XM_005276891.1:c.1387+4119_1387+4131del	XM_005276891.1:c.1387+4120_1387+4131del	XM_005276891.1:c.1387+4121_1387+4131del	XM_005276891.1:c.1387+4122_1387+4131del	XM_005276891.1:c.1387+4123_1387+4131del	XM_005276891.1:c.1387+4124_1387+4131del	XM_005276891.1:c.1387+4125_1387+4131del	XM_005276891.1:c.1387+4126_1387+4131del	XM_005276891.1:c.1387+4127_1387+4131del	XM_005276891.1:c.1387+4128_1387+4131del	XM_005276891.1:c.1387+4129_1387+4131del	XM_005276891.1:c.1387+4130_1387+4131del	XM_005276891.1:c.1387+4131del	XM_005276891.1:c.1387+4105=	XM_005276891.1:c.1387+4130_1387+4131dup	XM_005276891.1:c.1387+4129_1387+4131dup	XM_005276891.1:c.1387+4128_1387+4131dup	XM_005276891.1:c.1387+4127_1387+4131dup	XM_005276891.1:c.1387+4125_1387+4131dup	XM_005276891.1:c.1387+4123_1387+4131dup	XM_005276891.1:c.1387+4120_1387+4131dup
SOCS7 transcript variant X2	XM_005276892.1:c.1282+4131dup	XM_005276892.1:c.1282+4116_1282+4131del	XM_005276892.1:c.1282+4118_1282+4131del	XM_005276892.1:c.1282+4119_1282+4131del	XM_005276892.1:c.1282+4120_1282+4131del	XM_005276892.1:c.1282+4121_1282+4131del	XM_005276892.1:c.1282+4122_1282+4131del	XM_005276892.1:c.1282+4123_1282+4131del	XM_005276892.1:c.1282+4124_1282+4131del	XM_005276892.1:c.1282+4125_1282+4131del	XM_005276892.1:c.1282+4126_1282+4131del	XM_005276892.1:c.1282+4127_1282+4131del	XM_005276892.1:c.1282+4128_1282+4131del	XM_005276892.1:c.1282+4129_1282+4131del	XM_005276892.1:c.1282+4130_1282+4131del	XM_005276892.1:c.1282+4131del	XM_005276892.1:c.1282+4105=	XM_005276892.1:c.1282+4130_1282+4131dup	XM_005276892.1:c.1282+4129_1282+4131dup	XM_005276892.1:c.1282+4128_1282+4131dup	XM_005276892.1:c.1282+4127_1282+4131dup	XM_005276892.1:c.1282+4125_1282+4131dup	XM_005276892.1:c.1282+4123_1282+4131dup	XM_005276892.1:c.1282+4120_1282+4131dup
SOCS7 transcript variant X1	XM_017024551.2:c.1579+4105=	XM_017024551.2:c.1579+4116_1579+4132del	XM_017024551.2:c.1579+4118_1579+4132del	XM_017024551.2:c.1579+4119_1579+4132del	XM_017024551.2:c.1579+4120_1579+4132del	XM_017024551.2:c.1579+4121_1579+4132del	XM_017024551.2:c.1579+4122_1579+4132del	XM_017024551.2:c.1579+4123_1579+4132del	XM_017024551.2:c.1579+4124_1579+4132del	XM_017024551.2:c.1579+4125_1579+4132del	XM_017024551.2:c.1579+4126_1579+4132del	XM_017024551.2:c.1579+4127_1579+4132del	XM_017024551.2:c.1579+4128_1579+4132del	XM_017024551.2:c.1579+4129_1579+4132del	XM_017024551.2:c.1579+4130_1579+4132del	XM_017024551.2:c.1579+4131_1579+4132del	XM_017024551.2:c.1579+4132del	XM_017024551.2:c.1579+4132dup	XM_017024551.2:c.1579+4131_1579+4132dup	XM_017024551.2:c.1579+4130_1579+4132dup	XM_017024551.2:c.1579+4129_1579+4132dup	XM_017024551.2:c.1579+4127_1579+4132dup	XM_017024551.2:c.1579+4125_1579+4132dup	XM_017024551.2:c.1579+4122_1579+4132dup
SOCS7 transcript variant X2	XM_017024552.2:c.1474+4105=	XM_017024552.2:c.1474+4116_1474+4132del	XM_017024552.2:c.1474+4118_1474+4132del	XM_017024552.2:c.1474+4119_1474+4132del	XM_017024552.2:c.1474+4120_1474+4132del	XM_017024552.2:c.1474+4121_1474+4132del	XM_017024552.2:c.1474+4122_1474+4132del	XM_017024552.2:c.1474+4123_1474+4132del	XM_017024552.2:c.1474+4124_1474+4132del	XM_017024552.2:c.1474+4125_1474+4132del	XM_017024552.2:c.1474+4126_1474+4132del	XM_017024552.2:c.1474+4127_1474+4132del	XM_017024552.2:c.1474+4128_1474+4132del	XM_017024552.2:c.1474+4129_1474+4132del	XM_017024552.2:c.1474+4130_1474+4132del	XM_017024552.2:c.1474+4131_1474+4132del	XM_017024552.2:c.1474+4132del	XM_017024552.2:c.1474+4132dup	XM_017024552.2:c.1474+4131_1474+4132dup	XM_017024552.2:c.1474+4130_1474+4132dup	XM_017024552.2:c.1474+4129_1474+4132dup	XM_017024552.2:c.1474+4127_1474+4132dup	XM_017024552.2:c.1474+4125_1474+4132dup	XM_017024552.2:c.1474+4122_1474+4132dup

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#.

46 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95954686	Feb 05, 2009 (130)
2	SWEGEN	ss3015486954	Nov 08, 2017 (151)
3	URBANLAB	ss3650647909	Oct 12, 2018 (152)
4	KOGIC	ss3978793182	Apr 27, 2020 (154)
5	KOGIC	ss3978793183	Apr 27, 2020 (154)
6	KOGIC	ss3978793184	Apr 27, 2020 (154)
7	GNOMAD	ss4311064955	Apr 25, 2021 (155)
8	GNOMAD	ss4311064956	Apr 25, 2021 (155)
9	GNOMAD	ss4311064957	Apr 25, 2021 (155)
10	GNOMAD	ss4311064958	Apr 25, 2021 (155)
11	GNOMAD	ss4311064959	Apr 25, 2021 (155)
12	GNOMAD	ss4311064960	Apr 25, 2021 (155)
13	GNOMAD	ss4311064961	Apr 25, 2021 (155)
14	GNOMAD	ss4311064963	Apr 25, 2021 (155)
15	GNOMAD	ss4311064964	Apr 25, 2021 (155)
16	GNOMAD	ss4311064965	Apr 25, 2021 (155)
17	GNOMAD	ss4311064966	Apr 25, 2021 (155)
18	GNOMAD	ss4311064967	Apr 25, 2021 (155)
19	GNOMAD	ss4311064968	Apr 25, 2021 (155)
20	GNOMAD	ss4311064969	Apr 25, 2021 (155)
21	GNOMAD	ss4311064970	Apr 25, 2021 (155)
22	GNOMAD	ss4311064971	Apr 25, 2021 (155)
23	GNOMAD	ss4311064972	Apr 25, 2021 (155)
24	GNOMAD	ss4311064973	Apr 25, 2021 (155)
25	GNOMAD	ss4311064974	Apr 25, 2021 (155)
26	GNOMAD	ss4311064975	Apr 25, 2021 (155)
27	GNOMAD	ss4311064976	Apr 25, 2021 (155)
28	GNOMAD	ss4311064977	Apr 25, 2021 (155)
29	TOPMED	ss5034990847	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5222277569	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5222277570	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5222277571	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5222277572	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5222277573	Apr 25, 2021 (155)
35	TOMMO_GENOMICS	ss5222277574	Apr 25, 2021 (155)
36	HUGCELL_USP	ss5496099743	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5496099744	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5496099745	Oct 16, 2022 (156)
39	SANFORD_IMAGENETICS	ss5660048647	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5778439335	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5778439336	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5778439337	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5778439338	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5778439340	Oct 16, 2022 (156)
45	EVA	ss5833944378	Oct 16, 2022 (156)
46	EVA	ss5833944379	Oct 16, 2022 (156)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506391336 (NC_000017.11:38381946::A 628/16364) Row 506391337 (NC_000017.11:38381946::AA 1907/16618) Row 506391338 (NC_000017.11:38381946::AAA 479/16708)...	-	Apr 25, 2021 (155)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 35171183 (NC_000017.11:38381946::A 126/810) Row 35171184 (NC_000017.11:38381946::AA 159/810) Row 35171185 (NC_000017.11:38381946::AAA 35/810)	-	Apr 27, 2020 (154)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 35171183 (NC_000017.11:38381946::A 126/810) Row 35171184 (NC_000017.11:38381946::AA 159/810) Row 35171185 (NC_000017.11:38381946::AAA 35/810)	-	Apr 27, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 35171183 (NC_000017.11:38381946::A 126/810) Row 35171184 (NC_000017.11:38381946::AA 159/810) Row 35171185 (NC_000017.11:38381946::AAA 35/810)	-	Apr 27, 2020 (154)
72	8.3KJPN Submission ignored due to conflicting rows: Row 80246876 (NC_000017.10:36537772:A: 797/13810) Row 80246877 (NC_000017.10:36537772::AA 88/13810) Row 80246878 (NC_000017.10:36537772::A 39/13810)...	-	Apr 25, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 80246876 (NC_000017.10:36537772:A: 797/13810) Row 80246877 (NC_000017.10:36537772::AA 88/13810) Row 80246878 (NC_000017.10:36537772::A 39/13810)...	-	Apr 25, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 80246876 (NC_000017.10:36537772:A: 797/13810) Row 80246877 (NC_000017.10:36537772::AA 88/13810) Row 80246878 (NC_000017.10:36537772::A 39/13810)...	-	Apr 25, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 80246876 (NC_000017.10:36537772:A: 797/13810) Row 80246877 (NC_000017.10:36537772::AA 88/13810) Row 80246878 (NC_000017.10:36537772::A 39/13810)...	-	Apr 25, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 80246876 (NC_000017.10:36537772:A: 797/13810) Row 80246877 (NC_000017.10:36537772::AA 88/13810) Row 80246878 (NC_000017.10:36537772::A 39/13810)...	-	Apr 25, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 80246876 (NC_000017.10:36537772:A: 797/13810) Row 80246877 (NC_000017.10:36537772::AA 88/13810) Row 80246878 (NC_000017.10:36537772::A 39/13810)...	-	Apr 25, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 112276439 (NC_000017.11:38381946::AA 1424/24788) Row 112276440 (NC_000017.11:38381946::AAA 104/24788) Row 112276441 (NC_000017.11:38381946::A 279/24788)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 112276439 (NC_000017.11:38381946::AA 1424/24788) Row 112276440 (NC_000017.11:38381946::AAA 104/24788) Row 112276441 (NC_000017.11:38381946::A 279/24788)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 112276439 (NC_000017.11:38381946::AA 1424/24788) Row 112276440 (NC_000017.11:38381946::AAA 104/24788) Row 112276441 (NC_000017.11:38381946::A 279/24788)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 112276439 (NC_000017.11:38381946::AA 1424/24788) Row 112276440 (NC_000017.11:38381946::AAA 104/24788) Row 112276441 (NC_000017.11:38381946::A 279/24788)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 112276439 (NC_000017.11:38381946::AA 1424/24788) Row 112276440 (NC_000017.11:38381946::AAA 104/24788) Row 112276441 (NC_000017.11:38381946::A 279/24788)...	-	Oct 16, 2022 (156)
83	TopMed	NC_000017.11 - 38381947	Apr 25, 2021 (155)
84	ALFA	NC_000017.11 - 38381947	Apr 25, 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)
rs60321598	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4311064977	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4311064976	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4311064975	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
250536509, ss4311064974, ss5034990847	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5660048647	NC_000017.10:36537772:AAAAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA
ss4311064973	NC_000017.11:38381946:AAAAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4311064972	NC_000017.11:38381946:AAAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4311064971	NC_000017.11:38381946:AAAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4311064970	NC_000017.11:38381946:AAAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4311064969	NC_000017.11:38381946:AAAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064968	NC_000017.11:38381946:AAAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3015486954	NC_000017.10:36537772:AAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064967	NC_000017.11:38381946:AAAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064966	NC_000017.11:38381946:AAAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064965, ss5496099745	NC_000017.11:38381946:AAA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222277574	NC_000017.10:36537772:AA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064964	NC_000017.11:38381946:AA:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222277569	NC_000017.10:36537772:A:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064963, ss5778439338	NC_000017.11:38381946:A:	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222277571	NC_000017.10:36537772::A	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3978793182, ss4311064955, ss5496099743, ss5778439337	NC_000017.11:38381946::A	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222277570, ss5833944378	NC_000017.10:36537772::AA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3978793183, ss4311064956, ss5496099744, ss5778439335	NC_000017.11:38381946::AA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95954686	NT_010783.15:1811951::AA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222277573, ss5833944379	NC_000017.10:36537772::AAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3978793184, ss4311064957, ss5778439336	NC_000017.11:38381946::AAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3650647909	NC_000017.11:38381966::AAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5222277572	NC_000017.10:36537772::AAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064958, ss5778439340	NC_000017.11:38381946::AAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
223670321	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064959	NC_000017.11:38381946::AAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064960	NC_000017.11:38381946::AAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4311064961	NC_000017.11:38381946::AAAAAAAAAAA	NC_000017.11:38381946:AAAAAAAAAAAA… NC_000017.11:38381946:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs55949628

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

Genome context:

Select flank length:

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

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs55949628