Name: rs750111284
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.

rs750111284

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:132070012-132070024 (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(G)₇ / del(G)₆ / del(G)₅ / del(…
del(G)₇ / del(G)₆ / del(G)₅ / del(G)₄ / delGGG / delGG / delG / dupG / dupGG / dupGGG / dup(G)₄ / dup(G)₅ / dup(G)₆ / dup(G)₇ / dup(G)₈ / dup(G)₉ / dup(G)₁₀ / dup(G)₁₁ / dup(G)₁₂ / ins(G)₁₄ / ins(G)₁₅ / ins(G)₁₆ / ins(G)₁₇ / ins(G)₂₃ / ins(G)₃₁
Variation Type: Indel Insertion and Deletion
Frequency: del(G)₇=0.00000 (0/11822, ALFA)
del(G)₆=0.00000 (0/11822, ALFA)
del(G)₅=0.00000 (0/11822, ALFA) (+ 13 more)
del(G)₄=0.00000 (0/11822, ALFA)
delGGG=0.00000 (0/11822, ALFA)
delGG=0.00000 (0/11822, ALFA)
delG=0.00000 (0/11822, ALFA)
dupG=0.00000 (0/11822, ALFA)
dupGG=0.00000 (0/11822, ALFA)
dupGGG=0.00000 (0/11822, ALFA)
dup(G)₄=0.00000 (0/11822, ALFA)
dup(G)₅=0.00000 (0/11822, ALFA)
dup(G)₈=0.00000 (0/11822, ALFA)
dup(G)₉=0.00000 (0/11822, ALFA)
dup(G)₁₁=0.00000 (0/11822, ALFA)
dup(G)₁₂=0.00000 (0/11822, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HHLA1 : 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	HWEP
Total	Global	11822	GGGGGGGGGGGGG=1.00000	GGGGGG=0.00000, GGGGGGG=0.00000, GGGGGGGG=0.00000, GGGGGGGGG=0.00000, GGGGGGGGGG=0.00000, GGGGGGGGGGG=0.00000, GGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.00000	1.0	N/A
European	Sub	7586	GGGGGGGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	2810	GGGGGGGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African Others	Sub	108	GGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGG=0.000, GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
African American	Sub	2702	GGGGGGGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.0000	1.0	N/A
Asian	Sub	108	GGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGG=0.000, GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
East Asian	Sub	84	GGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	24	GGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 1	Sub	144	GGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGG=0.000, GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
Latin American 2	Sub	610	GGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGG=0.000, GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	94	GGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	470	GGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGG=0.000, GGGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11822	(G)₁₃=1.00000	del(G)₇=0.00000, del(G)₆=0.00000, del(G)₅=0.00000, del(G)₄=0.00000, delGGG=0.00000, delGG=0.00000, delG=0.00000, dupG=0.00000, dupGG=0.00000, dupGGG=0.00000, dup(G)₄=0.00000, dup(G)₅=0.00000, dup(G)₈=0.00000, dup(G)₉=0.00000, dup(G)₁₁=0.00000, dup(G)₁₂=0.00000
Allele Frequency Aggregator	European	Sub	7586	(G)₁₃=1.0000	del(G)₇=0.0000, del(G)₆=0.0000, del(G)₅=0.0000, del(G)₄=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000, dup(G)₈=0.0000, dup(G)₉=0.0000, dup(G)₁₁=0.0000, dup(G)₁₂=0.0000
Allele Frequency Aggregator	African	Sub	2810	(G)₁₃=1.0000	del(G)₇=0.0000, del(G)₆=0.0000, del(G)₅=0.0000, del(G)₄=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000, dup(G)₈=0.0000, dup(G)₉=0.0000, dup(G)₁₁=0.0000, dup(G)₁₂=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	(G)₁₃=1.000	del(G)₇=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000, dup(G)₈=0.000, dup(G)₉=0.000, dup(G)₁₁=0.000, dup(G)₁₂=0.000
Allele Frequency Aggregator	Other	Sub	470	(G)₁₃=1.000	del(G)₇=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000, dup(G)₈=0.000, dup(G)₉=0.000, dup(G)₁₁=0.000, dup(G)₁₂=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	(G)₁₃=1.000	del(G)₇=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000, dup(G)₈=0.000, dup(G)₉=0.000, dup(G)₁₁=0.000, dup(G)₁₂=0.000
Allele Frequency Aggregator	Asian	Sub	108	(G)₁₃=1.000	del(G)₇=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000, dup(G)₈=0.000, dup(G)₉=0.000, dup(G)₁₁=0.000, dup(G)₁₂=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(G)₁₃=1.00	del(G)₇=0.00, del(G)₆=0.00, del(G)₅=0.00, del(G)₄=0.00, delGGG=0.00, delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00, dup(G)₈=0.00, dup(G)₉=0.00, dup(G)₁₁=0.00, dup(G)₁₂=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 8	NC_000008.11:g.132070018_132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070019_132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070020_132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070021_132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070022_132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070023_132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070024del
GRCh38.p14 chr 8	NC_000008.11:g.132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070023_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070022_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070021_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070020_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070019_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070018_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070017_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070016_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070015_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070014_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070013_132070024dup
GRCh38.p14 chr 8	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGG
GRCh38.p14 chr 8	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGG
GRCh38.p14 chr 8	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGG
GRCh38.p14 chr 8	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 8	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 8	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082265_133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082266_133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082267_133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082268_133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082269_133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082270_133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082271del
GRCh37.p13 chr 8	NC_000008.10:g.133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082270_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082269_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082268_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082267_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082266_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082265_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082264_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082263_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082262_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082261_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082260_133082271dup
GRCh37.p13 chr 8	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Gene: HHLA1, HERV-H LTR-associating 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HHLA1 transcript	NM_001145095.3:c.1469+132… NM_001145095.3:c.1469+1322_1469+1328del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(G)₁₃=	del(G)₇	del(G)₆	del(G)₅	del(G)₄	delGGG	delGG	delG	dupG	dupGG	dupGGG	dup(G)₄	dup(G)₅	dup(G)₆	dup(G)₇	dup(G)₈	dup(G)₉	dup(G)₁₀	dup(G)₁₁	dup(G)₁₂	ins(G)₁₄	ins(G)₁₅	ins(G)₁₆	ins(G)₁₇	ins(G)₂₃	ins(G)₃₁
GRCh38.p14 chr 8	NC_000008.11:g.132070012_132070024=	NC_000008.11:g.132070018_132070024del	NC_000008.11:g.132070019_132070024del	NC_000008.11:g.132070020_132070024del	NC_000008.11:g.132070021_132070024del	NC_000008.11:g.132070022_132070024del	NC_000008.11:g.132070023_132070024del	NC_000008.11:g.132070024del	NC_000008.11:g.132070024dup	NC_000008.11:g.132070023_132070024dup	NC_000008.11:g.132070022_132070024dup	NC_000008.11:g.132070021_132070024dup	NC_000008.11:g.132070020_132070024dup	NC_000008.11:g.132070019_132070024dup	NC_000008.11:g.132070018_132070024dup	NC_000008.11:g.132070017_132070024dup	NC_000008.11:g.132070016_132070024dup	NC_000008.11:g.132070015_132070024dup	NC_000008.11:g.132070014_132070024dup	NC_000008.11:g.132070013_132070024dup	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGG	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGG	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGG	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGGG	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGGGGGGGGG	NC_000008.11:g.132070024_132070025insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 8	NC_000008.10:g.133082259_133082271=	NC_000008.10:g.133082265_133082271del	NC_000008.10:g.133082266_133082271del	NC_000008.10:g.133082267_133082271del	NC_000008.10:g.133082268_133082271del	NC_000008.10:g.133082269_133082271del	NC_000008.10:g.133082270_133082271del	NC_000008.10:g.133082271del	NC_000008.10:g.133082271dup	NC_000008.10:g.133082270_133082271dup	NC_000008.10:g.133082269_133082271dup	NC_000008.10:g.133082268_133082271dup	NC_000008.10:g.133082267_133082271dup	NC_000008.10:g.133082266_133082271dup	NC_000008.10:g.133082265_133082271dup	NC_000008.10:g.133082264_133082271dup	NC_000008.10:g.133082263_133082271dup	NC_000008.10:g.133082262_133082271dup	NC_000008.10:g.133082261_133082271dup	NC_000008.10:g.133082260_133082271dup	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGG	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGG	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGG	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGGG	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGGGGGGGGG	NC_000008.10:g.133082271_133082272insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
HHLA1 transcript	NM_001145095.1:c.1469+1328=	NM_001145095.1:c.1469+1322_1469+1328del	NM_001145095.1:c.1469+1323_1469+1328del	NM_001145095.1:c.1469+1324_1469+1328del	NM_001145095.1:c.1469+1325_1469+1328del	NM_001145095.1:c.1469+1326_1469+1328del	NM_001145095.1:c.1469+1327_1469+1328del	NM_001145095.1:c.1469+1328del	NM_001145095.1:c.1469+1328dup	NM_001145095.1:c.1469+1327_1469+1328dup	NM_001145095.1:c.1469+1326_1469+1328dup	NM_001145095.1:c.1469+1325_1469+1328dup	NM_001145095.1:c.1469+1324_1469+1328dup	NM_001145095.1:c.1469+1323_1469+1328dup	NM_001145095.1:c.1469+1322_1469+1328dup	NM_001145095.1:c.1469+1321_1469+1328dup	NM_001145095.1:c.1469+1320_1469+1328dup	NM_001145095.1:c.1469+1319_1469+1328dup	NM_001145095.1:c.1469+1318_1469+1328dup	NM_001145095.1:c.1469+1317_1469+1328dup	NM_001145095.1:c.1469+1328_1469+1329insCCCCCCCCCCCCCC	NM_001145095.1:c.1469+1328_1469+1329insCCCCCCCCCCCCCCC	NM_001145095.1:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCC	NM_001145095.1:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCCC	NM_001145095.1:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCCCCCCCCC	NM_001145095.1:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
HHLA1 transcript	NM_001145095.3:c.1469+1328=	NM_001145095.3:c.1469+1322_1469+1328del	NM_001145095.3:c.1469+1323_1469+1328del	NM_001145095.3:c.1469+1324_1469+1328del	NM_001145095.3:c.1469+1325_1469+1328del	NM_001145095.3:c.1469+1326_1469+1328del	NM_001145095.3:c.1469+1327_1469+1328del	NM_001145095.3:c.1469+1328del	NM_001145095.3:c.1469+1328dup	NM_001145095.3:c.1469+1327_1469+1328dup	NM_001145095.3:c.1469+1326_1469+1328dup	NM_001145095.3:c.1469+1325_1469+1328dup	NM_001145095.3:c.1469+1324_1469+1328dup	NM_001145095.3:c.1469+1323_1469+1328dup	NM_001145095.3:c.1469+1322_1469+1328dup	NM_001145095.3:c.1469+1321_1469+1328dup	NM_001145095.3:c.1469+1320_1469+1328dup	NM_001145095.3:c.1469+1319_1469+1328dup	NM_001145095.3:c.1469+1318_1469+1328dup	NM_001145095.3:c.1469+1317_1469+1328dup	NM_001145095.3:c.1469+1328_1469+1329insCCCCCCCCCCCCCC	NM_001145095.3:c.1469+1328_1469+1329insCCCCCCCCCCCCCCC	NM_001145095.3:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCC	NM_001145095.3:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCCC	NM_001145095.3:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCCCCCCCCC	NM_001145095.3:c.1469+1328_1469+1329insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC

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#.

47 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_UK10K_ALSPAC	ss1706259708	Apr 01, 2015 (144)
2	EVA_UK10K_TWINSUK	ss1706259716	Apr 01, 2015 (144)
3	EVA_UK10K_ALSPAC	ss1710405389	Apr 01, 2015 (144)
4	EVA_UK10K_TWINSUK	ss1710405449	Apr 01, 2015 (144)
5	SWEGEN	ss3004054187	Nov 08, 2017 (151)
6	SWEGEN	ss3004054188	Nov 08, 2017 (151)
7	SWEGEN	ss3004054189	Nov 08, 2017 (151)
8	SWEGEN	ss3004054190	Nov 08, 2017 (151)
9	SWEGEN	ss3004054191	Nov 08, 2017 (151)
10	SWEGEN	ss3004054192	Nov 08, 2017 (151)
11	EVA_DECODE	ss3723074424	Jul 13, 2019 (153)
12	EVA_DECODE	ss3723074425	Jul 13, 2019 (153)
13	EVA_DECODE	ss3723074426	Jul 13, 2019 (153)
14	EVA_DECODE	ss3723074427	Jul 13, 2019 (153)
15	EVA_DECODE	ss3723074428	Jul 13, 2019 (153)
16	EVA_DECODE	ss3723074429	Jul 13, 2019 (153)
17	PACBIO	ss3791521607	Jul 13, 2019 (153)
18	PACBIO	ss3791521608	Jul 13, 2019 (153)
19	PACBIO	ss3796403194	Jul 13, 2019 (153)
20	PACBIO	ss3796403195	Jul 13, 2019 (153)
21	EVA	ss3831431914	Apr 26, 2020 (154)
22	GNOMAD	ss4194041499	Apr 26, 2021 (155)
23	GNOMAD	ss4194041500	Apr 26, 2021 (155)
24	GNOMAD	ss4194041502	Apr 26, 2021 (155)
25	GNOMAD	ss4194041503	Apr 26, 2021 (155)
26	GNOMAD	ss4194041504	Apr 26, 2021 (155)
27	GNOMAD	ss4194041505	Apr 26, 2021 (155)
28	GNOMAD	ss4194041506	Apr 26, 2021 (155)
29	GNOMAD	ss4194041507	Apr 26, 2021 (155)
30	GNOMAD	ss4194041508	Apr 26, 2021 (155)
31	GNOMAD	ss4194041512	Apr 26, 2021 (155)
32	GNOMAD	ss4194041513	Apr 26, 2021 (155)
33	GNOMAD	ss4194041514	Apr 26, 2021 (155)
34	GNOMAD	ss4194041515	Apr 26, 2021 (155)
35	GNOMAD	ss4194041516	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5191152449	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5191152450	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5191152451	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5191152452	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5191152453	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5191152454	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5733919975	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5733919976	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5733919977	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5733919978	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5733919979	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5733919980	Oct 16, 2022 (156)
48	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 24629958 (NC_000008.10:133082258:GGGGG: 2614/3854) Row 24629959 (NC_000008.10:133082259:GGG: 509/3854)	-	Oct 12, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 24629958 (NC_000008.10:133082258:GGGGG: 2614/3854) Row 24629959 (NC_000008.10:133082259:GGG: 509/3854)	-	Oct 12, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 312154923 (NC_000008.11:132070011::G 2/9578) Row 312154924 (NC_000008.11:132070011::GG 2/9576) Row 312154926 (NC_000008.11:132070011::GGG 1/9576)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 49121756 (NC_000008.10:133082258::GGGGGGGG 112/12858) Row 49121757 (NC_000008.10:133082258::GGGGGGGGG 238/12858) Row 49121758 (NC_000008.10:133082258::GGGGGGG 152/12858)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 49121756 (NC_000008.10:133082258::GGGGGGGG 112/12858) Row 49121757 (NC_000008.10:133082258::GGGGGGGGG 238/12858) Row 49121758 (NC_000008.10:133082258::GGGGGGG 152/12858)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 49121756 (NC_000008.10:133082258::GGGGGGGG 112/12858) Row 49121757 (NC_000008.10:133082258::GGGGGGGGG 238/12858) Row 49121758 (NC_000008.10:133082258::GGGGGGG 152/12858)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 49121756 (NC_000008.10:133082258::GGGGGGGG 112/12858) Row 49121757 (NC_000008.10:133082258::GGGGGGGGG 238/12858) Row 49121758 (NC_000008.10:133082258::GGGGGGG 152/12858)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 49121756 (NC_000008.10:133082258::GGGGGGGG 112/12858) Row 49121757 (NC_000008.10:133082258::GGGGGGGGG 238/12858) Row 49121758 (NC_000008.10:133082258::GGGGGGG 152/12858)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 49121756 (NC_000008.10:133082258::GGGGGGGG 112/12858) Row 49121757 (NC_000008.10:133082258::GGGGGGGGG 238/12858) Row 49121758 (NC_000008.10:133082258::GGGGGGG 152/12858)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 67757079 (NC_000008.11:132070011::GGGGGGGGG 407/24040) Row 67757080 (NC_000008.11:132070011::GGGGGGGGGG 535/24040) Row 67757081 (NC_000008.11:132070011::GGGGGGGG 265/24040)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 67757079 (NC_000008.11:132070011::GGGGGGGGG 407/24040) Row 67757080 (NC_000008.11:132070011::GGGGGGGGGG 535/24040) Row 67757081 (NC_000008.11:132070011::GGGGGGGG 265/24040)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 67757079 (NC_000008.11:132070011::GGGGGGGGG 407/24040) Row 67757080 (NC_000008.11:132070011::GGGGGGGGGG 535/24040) Row 67757081 (NC_000008.11:132070011::GGGGGGGG 265/24040)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 67757079 (NC_000008.11:132070011::GGGGGGGGG 407/24040) Row 67757080 (NC_000008.11:132070011::GGGGGGGGGG 535/24040) Row 67757081 (NC_000008.11:132070011::GGGGGGGG 265/24040)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 67757079 (NC_000008.11:132070011::GGGGGGGGG 407/24040) Row 67757080 (NC_000008.11:132070011::GGGGGGGGGG 535/24040) Row 67757081 (NC_000008.11:132070011::GGGGGGGG 265/24040)...	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 67757079 (NC_000008.11:132070011::GGGGGGGGG 407/24040) Row 67757080 (NC_000008.11:132070011::GGGGGGGGGG 535/24040) Row 67757081 (NC_000008.11:132070011::GGGGGGGG 265/24040)...	-	Oct 16, 2022 (156)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 24629958 (NC_000008.10:133082258:GGGGG: 2522/3708) Row 24629959 (NC_000008.10:133082259:GGG: 471/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 24629958 (NC_000008.10:133082258:GGGGG: 2522/3708) Row 24629959 (NC_000008.10:133082259:GGG: 471/3708)	-	Oct 12, 2018 (152)
78	ALFA	NC_000008.11 - 132070012	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
ss4194041516	NC_000008.11:132070011:GGGGGGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGG	(self)
ss4194041515	NC_000008.11:132070011:GGGGGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGG	(self)
ss1706259708, ss1706259716	NC_000008.10:133082258:GGGGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGG	(self)
ss3723074429, ss4194041514	NC_000008.11:132070011:GGGGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGG	(self)
ss1710405389, ss1710405449	NC_000008.10:133082259:GGGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGG	(self)
ss4194041513	NC_000008.11:132070011:GGGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGG	(self)
	NC_000008.10:133082259:GGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGG	(self)
ss4194041512	NC_000008.11:132070011:GGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGG	(self)
ss3723074428	NC_000008.11:132070013:GGG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss4194041499	NC_000008.11:132070011::G	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3723074427	NC_000008.11:132070016::G	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss4194041500	NC_000008.11:132070011::GG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
ss4194041502	NC_000008.11:132070011::GGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss3723074426	NC_000008.11:132070016::GGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
ss3004054187	NC_000008.10:133082258::GGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG	(self)
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG	(self)
ss3004054189	NC_000008.10:133082258::GGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG	(self)
ss3723074425	NC_000008.11:132070016::GGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG	(self)
ss3004054191, ss5191152451	NC_000008.10:133082258::GGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG	(self)
ss5733919980	NC_000008.11:132070011::GGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG
ss3723074424	NC_000008.11:132070016::GGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG	(self)
ss3004054190, ss3791521607, ss3796403194, ss5191152449	NC_000008.10:133082258::GGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG	(self)
ss5733919977	NC_000008.11:132070011::GGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG	(self)
ss3004054188, ss3831431914, ss5191152450	NC_000008.10:133082258::GGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG	(self)
ss5733919975	NC_000008.11:132070011::GGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG	(self)
ss3004054192, ss3791521608, ss3796403195, ss5191152453	NC_000008.10:133082258::GGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5733919976	NC_000008.11:132070011::GGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGG
ss5191152452	NC_000008.10:133082258::GGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5733919978	NC_000008.11:132070011::GGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5191152454	NC_000008.10:133082258::GGGGGGGGGG… NC_000008.10:133082258::GGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5733919979	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG
10085378550	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4194041503	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4194041504	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4194041505	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4194041506	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4194041507	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4194041508	NC_000008.11:132070011::GGGGGGGGGG… NC_000008.11:132070011::GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3576668230	NC_000008.11:132070011::GGGG	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG
ss3576668233	NC_000008.11:132070011:G:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGGG
ss3576668234	NC_000008.11:132070011:GG:	NC_000008.11:132070011:GGGGGGGGGGG… NC_000008.11:132070011:GGGGGGGGGGGGG:GGGGGGGGGGG

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

No publications for rs750111284

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

rs750111284