Name: rs58961903
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.

rs58961903

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:112256187-112256215 (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)₁₆ / del(A)₁₅ / d…
del(A)₁₇ / del(A)₁₆ / 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)₅ / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₇=0.0000 (0/1036, ALFA)
del(A)₁₆=0.0000 (0/1036, ALFA)
del(A)₁₅=0.0000 (0/1036, ALFA) (+ 17 more)
del(A)₁₄=0.0000 (0/1036, ALFA)
del(A)₁₃=0.0000 (0/1036, ALFA)
del(A)₁₂=0.0000 (0/1036, ALFA)
del(A)₁₁=0.0000 (0/1036, ALFA)
del(A)₁₀=0.0000 (0/1036, ALFA)
del(A)₉=0.0000 (0/1036, ALFA)
del(A)₈=0.0000 (0/1036, ALFA)
del(A)₇=0.0000 (0/1036, ALFA)
del(A)₆=0.0000 (0/1036, ALFA)
del(A)₅=0.0000 (0/1036, ALFA)
del(A)₄=0.0000 (0/1036, ALFA)
delAAA=0.0000 (0/1036, ALFA)
delAA=0.0000 (0/1036, ALFA)
delA=0.0000 (0/1036, ALFA)
dupA=0.0000 (0/1036, ALFA)
dupAA=0.0000 (0/1036, ALFA)
dupAAA=0.0000 (0/1036, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LAMA4-AS1 : Intron Variant
LAMA4 : 2KB Upstream 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	1036	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	628	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	118	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	114	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	32	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	176	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	58	AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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	1036	(A)₂₉=1.0000	del(A)₁₇=0.0000, del(A)₁₆=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
Allele Frequency Aggregator	European	Sub	628	(A)₂₉=1.000	del(A)₁₇=0.000, del(A)₁₆=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
Allele Frequency Aggregator	Latin American 2	Sub	176	(A)₂₉=1.000	del(A)₁₇=0.000, del(A)₁₆=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
Allele Frequency Aggregator	African	Sub	118	(A)₂₉=1.000	del(A)₁₇=0.000, del(A)₁₆=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
Allele Frequency Aggregator	Other	Sub	58	(A)₂₉=1.00	del(A)₁₇=0.00, del(A)₁₆=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
Allele Frequency Aggregator	Asian	Sub	32	(A)₂₉=1.00	del(A)₁₇=0.00, del(A)₁₆=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
Allele Frequency Aggregator	Latin American 1	Sub	14	(A)₂₉=1.00	del(A)₁₇=0.00, del(A)₁₆=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
Allele Frequency Aggregator	South Asian	Sub	10	(A)₂₉=1.0	del(A)₁₇=0.0, del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0

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 6	NC_000006.12:g.112256199_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256200_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256201_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256202_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256203_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256204_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256205_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256206_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256207_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256208_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256209_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256210_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256211_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256212_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256213_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256214_112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256215del
GRCh38.p14 chr 6	NC_000006.12:g.112256215dup
GRCh38.p14 chr 6	NC_000006.12:g.112256214_112256215dup
GRCh38.p14 chr 6	NC_000006.12:g.112256213_112256215dup
GRCh38.p14 chr 6	NC_000006.12:g.112256212_112256215dup
GRCh38.p14 chr 6	NC_000006.12:g.112256211_112256215dup
GRCh38.p14 chr 6	NC_000006.12:g.112256209_112256215dup
GRCh37.p13 chr 6	NC_000006.11:g.112577401_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577402_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577403_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577404_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577405_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577406_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577407_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577408_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577409_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577410_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577411_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577412_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577413_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577414_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577415_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577416_112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577417del
GRCh37.p13 chr 6	NC_000006.11:g.112577417dup
GRCh37.p13 chr 6	NC_000006.11:g.112577416_112577417dup
GRCh37.p13 chr 6	NC_000006.11:g.112577415_112577417dup
GRCh37.p13 chr 6	NC_000006.11:g.112577414_112577417dup
GRCh37.p13 chr 6	NC_000006.11:g.112577413_112577417dup
GRCh37.p13 chr 6	NC_000006.11:g.112577411_112577417dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3424_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3425_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3426_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3427_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3428_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3429_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3430_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3431_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3432_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3433_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3434_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3435_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3436_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3437_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3438_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3439_3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3440del
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3440dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3439_3440dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3438_3440dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3437_3440dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3436_3440dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3434_3440dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253720_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253721_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253722_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253723_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253724_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253725_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253726_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253727_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253728_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253729_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253730_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253731_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253732_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253733_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253734_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253735_253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253736del
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253736dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253735_253736dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253734_253736dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253733_253736dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253732_253736dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253730_253736dup

Gene: LAMA4, laminin subunit alpha 4 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LAMA4 transcript variant 1	NM_001105206.3:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant 3	NM_001105207.3:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant 4	NM_001105208.3:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant 5	NM_001105209.3:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant 2	NM_002290.5:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant X1	XM_005266983.5:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant X2	XM_005266984.5:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant X4	XM_017010854.3:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant X3	XM_047418769.1:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant X5	XM_047418770.1:c.	N/A	Upstream Transcript Variant
LAMA4 transcript variant X6	XM_047418771.1:c.	N/A	Upstream Transcript Variant

Gene: LAMA4-AS1, LAMA4 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LAMA4-AS1 transcript	NR_121193.1:n.	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	(A)₂₉=	del(A)₁₇	del(A)₁₆	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)₅	dup(A)₇
GRCh38.p14 chr 6	NC_000006.12:g.112256187_112256215=	NC_000006.12:g.112256199_112256215del	NC_000006.12:g.112256200_112256215del	NC_000006.12:g.112256201_112256215del	NC_000006.12:g.112256202_112256215del	NC_000006.12:g.112256203_112256215del	NC_000006.12:g.112256204_112256215del	NC_000006.12:g.112256205_112256215del	NC_000006.12:g.112256206_112256215del	NC_000006.12:g.112256207_112256215del	NC_000006.12:g.112256208_112256215del	NC_000006.12:g.112256209_112256215del	NC_000006.12:g.112256210_112256215del	NC_000006.12:g.112256211_112256215del	NC_000006.12:g.112256212_112256215del	NC_000006.12:g.112256213_112256215del	NC_000006.12:g.112256214_112256215del	NC_000006.12:g.112256215del	NC_000006.12:g.112256215dup	NC_000006.12:g.112256214_112256215dup	NC_000006.12:g.112256213_112256215dup	NC_000006.12:g.112256212_112256215dup	NC_000006.12:g.112256211_112256215dup	NC_000006.12:g.112256209_112256215dup
GRCh37.p13 chr 6	NC_000006.11:g.112577389_112577417=	NC_000006.11:g.112577401_112577417del	NC_000006.11:g.112577402_112577417del	NC_000006.11:g.112577403_112577417del	NC_000006.11:g.112577404_112577417del	NC_000006.11:g.112577405_112577417del	NC_000006.11:g.112577406_112577417del	NC_000006.11:g.112577407_112577417del	NC_000006.11:g.112577408_112577417del	NC_000006.11:g.112577409_112577417del	NC_000006.11:g.112577410_112577417del	NC_000006.11:g.112577411_112577417del	NC_000006.11:g.112577412_112577417del	NC_000006.11:g.112577413_112577417del	NC_000006.11:g.112577414_112577417del	NC_000006.11:g.112577415_112577417del	NC_000006.11:g.112577416_112577417del	NC_000006.11:g.112577417del	NC_000006.11:g.112577417dup	NC_000006.11:g.112577416_112577417dup	NC_000006.11:g.112577415_112577417dup	NC_000006.11:g.112577414_112577417dup	NC_000006.11:g.112577413_112577417dup	NC_000006.11:g.112577411_112577417dup
LAMA4 RefSeqGene (LRG_433)	NG_008209.1:g.3412_3440=	NG_008209.1:g.3424_3440del	NG_008209.1:g.3425_3440del	NG_008209.1:g.3426_3440del	NG_008209.1:g.3427_3440del	NG_008209.1:g.3428_3440del	NG_008209.1:g.3429_3440del	NG_008209.1:g.3430_3440del	NG_008209.1:g.3431_3440del	NG_008209.1:g.3432_3440del	NG_008209.1:g.3433_3440del	NG_008209.1:g.3434_3440del	NG_008209.1:g.3435_3440del	NG_008209.1:g.3436_3440del	NG_008209.1:g.3437_3440del	NG_008209.1:g.3438_3440del	NG_008209.1:g.3439_3440del	NG_008209.1:g.3440del	NG_008209.1:g.3440dup	NG_008209.1:g.3439_3440dup	NG_008209.1:g.3438_3440dup	NG_008209.1:g.3437_3440dup	NG_008209.1:g.3436_3440dup	NG_008209.1:g.3434_3440dup
GRCh37.p13 chr 6 fix patch HG1304_PATCH	NW_003871062.1:g.253708_253736=	NW_003871062.1:g.253720_253736del	NW_003871062.1:g.253721_253736del	NW_003871062.1:g.253722_253736del	NW_003871062.1:g.253723_253736del	NW_003871062.1:g.253724_253736del	NW_003871062.1:g.253725_253736del	NW_003871062.1:g.253726_253736del	NW_003871062.1:g.253727_253736del	NW_003871062.1:g.253728_253736del	NW_003871062.1:g.253729_253736del	NW_003871062.1:g.253730_253736del	NW_003871062.1:g.253731_253736del	NW_003871062.1:g.253732_253736del	NW_003871062.1:g.253733_253736del	NW_003871062.1:g.253734_253736del	NW_003871062.1:g.253735_253736del	NW_003871062.1:g.253736del	NW_003871062.1:g.253736dup	NW_003871062.1:g.253735_253736dup	NW_003871062.1:g.253734_253736dup	NW_003871062.1:g.253733_253736dup	NW_003871062.1:g.253732_253736dup	NW_003871062.1:g.253730_253736dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

50 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80525293	Dec 15, 2007 (129)
2	HGSV	ss82249642	Dec 15, 2007 (129)
3	HUMANGENOME_JCVI	ss98459683	Mar 15, 2016 (147)
4	PJP	ss295301602	Aug 21, 2014 (142)
5	EVA_GENOME_DK	ss1576836860	Apr 09, 2015 (144)
6	EVA_GENOME_DK	ss1578545274	Apr 09, 2015 (144)
7	SWEGEN	ss2999766439	Oct 12, 2018 (152)
8	EVA_DECODE	ss3718052736	Jul 13, 2019 (153)
9	EVA_DECODE	ss3718052737	Jul 13, 2019 (153)
10	EVA_DECODE	ss3718052738	Jul 13, 2019 (153)
11	EVA_DECODE	ss3718052739	Jul 13, 2019 (153)
12	EVA_DECODE	ss3718052740	Jul 13, 2019 (153)
13	EVA_DECODE	ss3718052741	Jul 13, 2019 (153)
14	ACPOP	ss3733881664	Jul 13, 2019 (153)
15	ACPOP	ss3733881665	Jul 13, 2019 (153)
16	ACPOP	ss3733881666	Jul 13, 2019 (153)
17	ACPOP	ss3733881667	Jul 13, 2019 (153)
18	PACBIO	ss3790923099	Jul 13, 2019 (153)
19	PACBIO	ss3790923100	Jul 13, 2019 (153)
20	PACBIO	ss3795802298	Jul 13, 2019 (153)
21	PACBIO	ss3795802299	Jul 13, 2019 (153)
22	EVA	ss3830138645	Apr 26, 2020 (154)
23	GNOMAD	ss4149369242	Apr 26, 2021 (155)
24	GNOMAD	ss4149369243	Apr 26, 2021 (155)
25	GNOMAD	ss4149369244	Apr 26, 2021 (155)
26	GNOMAD	ss4149369245	Apr 26, 2021 (155)
27	GNOMAD	ss4149369246	Apr 26, 2021 (155)
28	GNOMAD	ss4149369247	Apr 26, 2021 (155)
29	GNOMAD	ss4149369248	Apr 26, 2021 (155)
30	GNOMAD	ss4149369249	Apr 26, 2021 (155)
31	GNOMAD	ss4149369250	Apr 26, 2021 (155)
32	GNOMAD	ss4149369251	Apr 26, 2021 (155)
33	GNOMAD	ss4149369252	Apr 26, 2021 (155)
34	GNOMAD	ss4149369253	Apr 26, 2021 (155)
35	GNOMAD	ss4149369254	Apr 26, 2021 (155)
36	GNOMAD	ss4149369255	Apr 26, 2021 (155)
37	GNOMAD	ss4149369256	Apr 26, 2021 (155)
38	GNOMAD	ss4149369257	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5179409705	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5179409706	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5179409707	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5179409708	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5179409709	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5269944872	Oct 13, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5269944873	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5718151718	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5718151719	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5718151720	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5718151721	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5718151722	Oct 13, 2022 (156)
51	The Danish reference pan genome Submission ignored due to conflicting rows: Row 95478 (NC_000006.11:112577388:AAAAAAAAAAAAAAAAA: 40/40) Row 1101341 (NC_000006.11:112577388:AAAAA: 11/40)	-	Apr 26, 2020 (154)
52	The Danish reference pan genome Submission ignored due to conflicting rows: Row 95478 (NC_000006.11:112577388:AAAAAAAAAAAAAAAAA: 40/40) Row 1101341 (NC_000006.11:112577388:AAAAA: 11/40)	-	Apr 26, 2020 (154)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 237700508 (NC_000006.12:112256186::A 701/65054) Row 237700509 (NC_000006.12:112256186::AA 53/65076) Row 237700510 (NC_000006.12:112256186::AAA 7/65076)...	-	Apr 26, 2021 (155)
69	Northern Sweden Submission ignored due to conflicting rows: Row 7166529 (NC_000006.11:112577388:AAAAA: 105/550) Row 7166530 (NC_000006.11:112577388:AA: 57/550) Row 7166531 (NC_000006.11:112577388:AAA: 21/550)...	-	Jul 13, 2019 (153)
70	Northern Sweden Submission ignored due to conflicting rows: Row 7166529 (NC_000006.11:112577388:AAAAA: 105/550) Row 7166530 (NC_000006.11:112577388:AA: 57/550) Row 7166531 (NC_000006.11:112577388:AAA: 21/550)...	-	Jul 13, 2019 (153)
71	Northern Sweden Submission ignored due to conflicting rows: Row 7166529 (NC_000006.11:112577388:AAAAA: 105/550) Row 7166530 (NC_000006.11:112577388:AA: 57/550) Row 7166531 (NC_000006.11:112577388:AAA: 21/550)...	-	Jul 13, 2019 (153)
72	Northern Sweden Submission ignored due to conflicting rows: Row 7166529 (NC_000006.11:112577388:AAAAA: 105/550) Row 7166530 (NC_000006.11:112577388:AA: 57/550) Row 7166531 (NC_000006.11:112577388:AAA: 21/550)...	-	Jul 13, 2019 (153)
73	8.3KJPN Submission ignored due to conflicting rows: Row 37379012 (NC_000006.11:112577388:AA: 3023/16196) Row 37379013 (NC_000006.11:112577388::A 32/16196) Row 37379014 (NC_000006.11:112577388:AAA: 763/16196)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 37379012 (NC_000006.11:112577388:AA: 3023/16196) Row 37379013 (NC_000006.11:112577388::A 32/16196) Row 37379014 (NC_000006.11:112577388:AAA: 763/16196)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 37379012 (NC_000006.11:112577388:AA: 3023/16196) Row 37379013 (NC_000006.11:112577388::A 32/16196) Row 37379014 (NC_000006.11:112577388:AAA: 763/16196)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 37379012 (NC_000006.11:112577388:AA: 3023/16196) Row 37379013 (NC_000006.11:112577388::A 32/16196) Row 37379014 (NC_000006.11:112577388:AAA: 763/16196)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 37379012 (NC_000006.11:112577388:AA: 3023/16196) Row 37379013 (NC_000006.11:112577388::A 32/16196) Row 37379014 (NC_000006.11:112577388:AAA: 763/16196)...	-	Apr 26, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 51988822 (NC_000006.12:112256186:AA: 6943/27538) Row 51988823 (NC_000006.12:112256186::A 70/27538) Row 51988824 (NC_000006.12:112256186:AAA: 1677/27538)...	-	Oct 13, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 51988822 (NC_000006.12:112256186:AA: 6943/27538) Row 51988823 (NC_000006.12:112256186::A 70/27538) Row 51988824 (NC_000006.12:112256186:AAA: 1677/27538)...	-	Oct 13, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 51988822 (NC_000006.12:112256186:AA: 6943/27538) Row 51988823 (NC_000006.12:112256186::A 70/27538) Row 51988824 (NC_000006.12:112256186:AAA: 1677/27538)...	-	Oct 13, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 51988822 (NC_000006.12:112256186:AA: 6943/27538) Row 51988823 (NC_000006.12:112256186::A 70/27538) Row 51988824 (NC_000006.12:112256186:AAA: 1677/27538)...	-	Oct 13, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 51988822 (NC_000006.12:112256186:AA: 6943/27538) Row 51988823 (NC_000006.12:112256186::A 70/27538) Row 51988824 (NC_000006.12:112256186:AAA: 1677/27538)...	-	Oct 13, 2022 (156)
83	ALFA	NC_000006.12 - 112256187	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)
rs68169992	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1578545274	NC_000006.11:112577388:AAAAAAAAAAA… NC_000006.11:112577388:AAAAAAAAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4149369257	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4149369256	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4149369255	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4149369254	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4149369253	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4149369252	NC_000006.12:112256186:AAAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4149369251	NC_000006.12:112256186:AAAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4149369250	NC_000006.12:112256186:AAAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4149369249	NC_000006.12:112256186:AAAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369248	NC_000006.12:112256186:AAAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss2999766439	NC_000006.11:112577388:AAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718052741, ss5269944873	NC_000006.12:112256186:AAAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss1576836860, ss3733881664	NC_000006.11:112577388:AAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718052740	NC_000006.12:112256187:AAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3733881667, ss3790923099, ss3795802298, ss5179409709	NC_000006.11:112577388:AAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5269944872, ss5718151722	NC_000006.12:112256186:AAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718052739	NC_000006.12:112256188:AAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3733881666, ss5179409707	NC_000006.11:112577388:AAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5718151720	NC_000006.12:112256186:AAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718052738	NC_000006.12:112256189:AAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80525293, ss82249642	NC_000006.9:112684108:AA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss295301602	NC_000006.10:112684081:AA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3733881665, ss3790923100, ss3795802299, ss3830138645, ss5179409705	NC_000006.11:112577388:AA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5718151718	NC_000006.12:112256186:AA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718052737	NC_000006.12:112256190:AA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss98459683	NT_025741.15:16746845:AA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5179409708	NC_000006.11:112577388:A:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5718151721	NC_000006.12:112256186:A:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718052736	NC_000006.12:112256191:A:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5179409706	NC_000006.11:112577388::A	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369242, ss5718151719	NC_000006.12:112256186::A	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369243	NC_000006.12:112256186::AA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369244	NC_000006.12:112256186::AAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
7663333042	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369245	NC_000006.12:112256186::AAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369246	NC_000006.12:112256186::AAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4149369247	NC_000006.12:112256186::AAAAAAA	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3508828793	NC_000006.12:112256186:AAAAA:	NC_000006.12:112256186:AAAAAAAAAAA… NC_000006.12:112256186:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA

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

No publications for rs58961903

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

rs58961903