Name: rs56383997
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.

rs56383997

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:104488741-104488772 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(GT)₁₀ / del(GT)₉ / del(GT)₈ / …
del(GT)₁₀ / del(GT)₉ / del(GT)₈ / del(GT)₇ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆
Variation Type: Indel Insertion and Deletion
Frequency: (GT)₁₆=0.2766 (1385/5008, 1000G)
(GT)₁₆=0.3502 (1730/4940, ALFA)
delGTGT=0.2937 (1132/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CHST11 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	4940	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.3502	GTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0097, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1245, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.4619, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0099, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0267, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0170, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.25989	0.362751	0.377358	32
European	Sub	4836	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.3373	GTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0097, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1270, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.4717, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0101, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0269, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0174, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.237139	0.373902	0.388959	35
African	Sub	68	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	4	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
African American	Sub	64	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	GTGTGTGTGTGT=0, GTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
East Asian	Sub	0	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	GTGTGTGTGTGT=0, GTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Other Asian	Sub	0	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	GTGTGTGTGTGT=0, GTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 1	Sub	0	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	GTGTGTGTGTGT=0, GTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 2	Sub	10	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	4	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	GTGTGTGTGTGT=0.0, GTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other	Sub	22	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.77	GTGTGTGTGTGT=0.00, GTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGT=0.05, GTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.05, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.05, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.09, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(GT)₁₆=0.2766	delGT=0.7234
1000Genomes	African	Sub	1322	(GT)₁₆=0.3994	delGT=0.6006
1000Genomes	East Asian	Sub	1008	(GT)₁₆=0.0298	delGT=0.9702
1000Genomes	Europe	Sub	1006	(GT)₁₆=0.3598	delGT=0.6402
1000Genomes	South Asian	Sub	978	(GT)₁₆=0.257	delGT=0.743
1000Genomes	American	Sub	694	(GT)₁₆=0.308	delGT=0.692
Allele Frequency Aggregator	Total	Global	4940	(GT)₁₆=0.3502	del(GT)₁₀=0.0000, del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0097, delGTGT=0.1245, delGT=0.4619, dupGT=0.0267, dupGTGT=0.0170, dup(GT)₃=0.0099, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000
Allele Frequency Aggregator	European	Sub	4836	(GT)₁₆=0.3373	del(GT)₁₀=0.0000, del(GT)₉=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0097, delGTGT=0.1270, delGT=0.4717, dupGT=0.0269, dupGTGT=0.0174, dup(GT)₃=0.0101, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000
Allele Frequency Aggregator	African	Sub	68	(GT)₁₆=1.00	del(GT)₁₀=0.00, del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00
Allele Frequency Aggregator	Other	Sub	22	(GT)₁₆=0.77	del(GT)₁₀=0.00, del(GT)₉=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.05, delGTGT=0.05, delGT=0.05, dupGT=0.09, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	10	(GT)₁₆=1.0	del(GT)₁₀=0.0, del(GT)₉=0.0, del(GT)₈=0.0, del(GT)₇=0.0, del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(GT)₁₆=1.0	del(GT)₁₀=0.0, del(GT)₉=0.0, del(GT)₈=0.0, del(GT)₇=0.0, del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(GT)₁₆=0	del(GT)₁₀=0, del(GT)₉=0, del(GT)₈=0, del(GT)₇=0, del(GT)₆=0, del(GT)₅=0, del(GT)₄=0, del(GT)₃=0, delGTGT=0, delGT=0, dupGT=0, dupGTGT=0, dup(GT)₃=0, dup(GT)₄=0, dup(GT)₅=0, dup(GT)₆=0
Allele Frequency Aggregator	Asian	Sub	0	(GT)₁₆=0	del(GT)₁₀=0, del(GT)₉=0, del(GT)₈=0, del(GT)₇=0, del(GT)₆=0, del(GT)₅=0, del(GT)₄=0, del(GT)₃=0, delGTGT=0, delGT=0, dupGT=0, dupGTGT=0, dup(GT)₃=0, dup(GT)₄=0, dup(GT)₅=0, dup(GT)₆=0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(GT)₁₆=0.7063	delGTGT=0.2937

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 12	NC_000012.12:g.104488741GT[6]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[7]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[8]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[9]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[10]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[11]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[12]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[13]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[14]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[15]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[17]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[18]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[19]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[20]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[21]
GRCh38.p14 chr 12	NC_000012.12:g.104488741GT[22]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[6]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[7]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[8]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[9]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[10]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[11]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[12]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[13]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[14]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[15]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[17]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[18]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[19]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[20]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[21]
GRCh37.p13 chr 12	NC_000012.11:g.104882519GT[22]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[6]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[7]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[8]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[9]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[10]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[11]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[12]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[13]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[14]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[15]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[17]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[18]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[19]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[20]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[21]
CHST11 RefSeqGene	NG_029810.2:g.36828GT[22]

Gene: CHST11, carbohydrate sulfotransferase 11 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CHST11 transcript variant 2	NM_001173982.2:c.103+3122… NM_001173982.2:c.103+31227GT[6]	N/A	Intron Variant
CHST11 transcript variant 1	NM_018413.6:c.118+31212GT… NM_018413.6:c.118+31212GT[6]	N/A	Intron Variant
CHST11 transcript variant X1	XM_047428914.1:c.-34+3121… XM_047428914.1:c.-34+31212GT[6]	N/A	Intron Variant
CHST11 transcript variant X2	XM_047428915.1:c.-34+3122… XM_047428915.1:c.-34+31227GT[6]	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	(GT)₁₆=	del(GT)₁₀	del(GT)₉	del(GT)₈	del(GT)₇	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆
GRCh38.p14 chr 12	NC_000012.12:g.104488741_104488772=	NC_000012.12:g.104488741GT[6]	NC_000012.12:g.104488741GT[7]	NC_000012.12:g.104488741GT[8]	NC_000012.12:g.104488741GT[9]	NC_000012.12:g.104488741GT[10]	NC_000012.12:g.104488741GT[11]	NC_000012.12:g.104488741GT[12]	NC_000012.12:g.104488741GT[13]	NC_000012.12:g.104488741GT[14]	NC_000012.12:g.104488741GT[15]	NC_000012.12:g.104488741GT[17]	NC_000012.12:g.104488741GT[18]	NC_000012.12:g.104488741GT[19]	NC_000012.12:g.104488741GT[20]	NC_000012.12:g.104488741GT[21]	NC_000012.12:g.104488741GT[22]
GRCh37.p13 chr 12	NC_000012.11:g.104882519_104882550=	NC_000012.11:g.104882519GT[6]	NC_000012.11:g.104882519GT[7]	NC_000012.11:g.104882519GT[8]	NC_000012.11:g.104882519GT[9]	NC_000012.11:g.104882519GT[10]	NC_000012.11:g.104882519GT[11]	NC_000012.11:g.104882519GT[12]	NC_000012.11:g.104882519GT[13]	NC_000012.11:g.104882519GT[14]	NC_000012.11:g.104882519GT[15]	NC_000012.11:g.104882519GT[17]	NC_000012.11:g.104882519GT[18]	NC_000012.11:g.104882519GT[19]	NC_000012.11:g.104882519GT[20]	NC_000012.11:g.104882519GT[21]	NC_000012.11:g.104882519GT[22]
CHST11 RefSeqGene	NG_029810.2:g.36828_36859=	NG_029810.2:g.36828GT[6]	NG_029810.2:g.36828GT[7]	NG_029810.2:g.36828GT[8]	NG_029810.2:g.36828GT[9]	NG_029810.2:g.36828GT[10]	NG_029810.2:g.36828GT[11]	NG_029810.2:g.36828GT[12]	NG_029810.2:g.36828GT[13]	NG_029810.2:g.36828GT[14]	NG_029810.2:g.36828GT[15]	NG_029810.2:g.36828GT[17]	NG_029810.2:g.36828GT[18]	NG_029810.2:g.36828GT[19]	NG_029810.2:g.36828GT[20]	NG_029810.2:g.36828GT[21]	NG_029810.2:g.36828GT[22]
CHST11 transcript variant 2	NM_001173982.1:c.103+31227=	NM_001173982.1:c.103+31227GT[6]	NM_001173982.1:c.103+31227GT[7]	NM_001173982.1:c.103+31227GT[8]	NM_001173982.1:c.103+31227GT[9]	NM_001173982.1:c.103+31227GT[10]	NM_001173982.1:c.103+31227GT[11]	NM_001173982.1:c.103+31227GT[12]	NM_001173982.1:c.103+31227GT[13]	NM_001173982.1:c.103+31227GT[14]	NM_001173982.1:c.103+31227GT[15]	NM_001173982.1:c.103+31227GT[17]	NM_001173982.1:c.103+31227GT[18]	NM_001173982.1:c.103+31227GT[19]	NM_001173982.1:c.103+31227GT[20]	NM_001173982.1:c.103+31227GT[21]	NM_001173982.1:c.103+31227GT[22]
CHST11 transcript variant 2	NM_001173982.2:c.103+31227=	NM_001173982.2:c.103+31227GT[6]	NM_001173982.2:c.103+31227GT[7]	NM_001173982.2:c.103+31227GT[8]	NM_001173982.2:c.103+31227GT[9]	NM_001173982.2:c.103+31227GT[10]	NM_001173982.2:c.103+31227GT[11]	NM_001173982.2:c.103+31227GT[12]	NM_001173982.2:c.103+31227GT[13]	NM_001173982.2:c.103+31227GT[14]	NM_001173982.2:c.103+31227GT[15]	NM_001173982.2:c.103+31227GT[17]	NM_001173982.2:c.103+31227GT[18]	NM_001173982.2:c.103+31227GT[19]	NM_001173982.2:c.103+31227GT[20]	NM_001173982.2:c.103+31227GT[21]	NM_001173982.2:c.103+31227GT[22]
CHST11 transcript variant 1	NM_018413.5:c.118+31212=	NM_018413.5:c.118+31212GT[6]	NM_018413.5:c.118+31212GT[7]	NM_018413.5:c.118+31212GT[8]	NM_018413.5:c.118+31212GT[9]	NM_018413.5:c.118+31212GT[10]	NM_018413.5:c.118+31212GT[11]	NM_018413.5:c.118+31212GT[12]	NM_018413.5:c.118+31212GT[13]	NM_018413.5:c.118+31212GT[14]	NM_018413.5:c.118+31212GT[15]	NM_018413.5:c.118+31212GT[17]	NM_018413.5:c.118+31212GT[18]	NM_018413.5:c.118+31212GT[19]	NM_018413.5:c.118+31212GT[20]	NM_018413.5:c.118+31212GT[21]	NM_018413.5:c.118+31212GT[22]
CHST11 transcript variant 1	NM_018413.6:c.118+31212=	NM_018413.6:c.118+31212GT[6]	NM_018413.6:c.118+31212GT[7]	NM_018413.6:c.118+31212GT[8]	NM_018413.6:c.118+31212GT[9]	NM_018413.6:c.118+31212GT[10]	NM_018413.6:c.118+31212GT[11]	NM_018413.6:c.118+31212GT[12]	NM_018413.6:c.118+31212GT[13]	NM_018413.6:c.118+31212GT[14]	NM_018413.6:c.118+31212GT[15]	NM_018413.6:c.118+31212GT[17]	NM_018413.6:c.118+31212GT[18]	NM_018413.6:c.118+31212GT[19]	NM_018413.6:c.118+31212GT[20]	NM_018413.6:c.118+31212GT[21]	NM_018413.6:c.118+31212GT[22]
CHST11 transcript variant X1	XM_047428914.1:c.-34+31212=	XM_047428914.1:c.-34+31212GT[6]	XM_047428914.1:c.-34+31212GT[7]	XM_047428914.1:c.-34+31212GT[8]	XM_047428914.1:c.-34+31212GT[9]	XM_047428914.1:c.-34+31212GT[10]	XM_047428914.1:c.-34+31212GT[11]	XM_047428914.1:c.-34+31212GT[12]	XM_047428914.1:c.-34+31212GT[13]	XM_047428914.1:c.-34+31212GT[14]	XM_047428914.1:c.-34+31212GT[15]	XM_047428914.1:c.-34+31212GT[17]	XM_047428914.1:c.-34+31212GT[18]	XM_047428914.1:c.-34+31212GT[19]	XM_047428914.1:c.-34+31212GT[20]	XM_047428914.1:c.-34+31212GT[21]	XM_047428914.1:c.-34+31212GT[22]
CHST11 transcript variant X2	XM_047428915.1:c.-34+31227=	XM_047428915.1:c.-34+31227GT[6]	XM_047428915.1:c.-34+31227GT[7]	XM_047428915.1:c.-34+31227GT[8]	XM_047428915.1:c.-34+31227GT[9]	XM_047428915.1:c.-34+31227GT[10]	XM_047428915.1:c.-34+31227GT[11]	XM_047428915.1:c.-34+31227GT[12]	XM_047428915.1:c.-34+31227GT[13]	XM_047428915.1:c.-34+31227GT[14]	XM_047428915.1:c.-34+31227GT[15]	XM_047428915.1:c.-34+31227GT[17]	XM_047428915.1:c.-34+31227GT[18]	XM_047428915.1:c.-34+31227GT[19]	XM_047428915.1:c.-34+31227GT[20]	XM_047428915.1:c.-34+31227GT[21]	XM_047428915.1:c.-34+31227GT[22]

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#.

74 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77883639	Jan 10, 2018 (151)
2	HUMANGENOME_JCVI	ss95606503	Feb 04, 2009 (130)
3	GMI	ss289149912	May 04, 2012 (137)
4	GMI	ss289149913	May 04, 2012 (137)
5	1000GENOMES	ss327574901	May 09, 2011 (137)
6	BILGI_BIOE	ss666582591	Apr 25, 2013 (138)
7	1000GENOMES	ss1372557880	Aug 21, 2014 (142)
8	DDI	ss1536741105	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1707607398	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1707607694	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710577654	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710577669	Apr 01, 2015 (144)
13	SWEGEN	ss3010277251	Nov 08, 2017 (151)
14	MCHAISSO	ss3063744109	Jan 10, 2018 (151)
15	MCHAISSO	ss3063744110	Jan 10, 2018 (151)
16	MCHAISSO	ss3064574247	Jan 10, 2018 (151)
17	MCHAISSO	ss3064574248	Jan 10, 2018 (151)
18	MCHAISSO	ss3065495452	Jan 10, 2018 (151)
19	MCHAISSO	ss3065495453	Jan 10, 2018 (151)
20	MCHAISSO	ss3065495454	Jan 10, 2018 (151)
21	EVA_DECODE	ss3694378010	Jul 13, 2019 (153)
22	EVA_DECODE	ss3694378011	Jul 13, 2019 (153)
23	EVA_DECODE	ss3694378012	Jul 13, 2019 (153)
24	EVA_DECODE	ss3694378013	Jul 13, 2019 (153)
25	EVA_DECODE	ss3694378014	Jul 13, 2019 (153)
26	EVA_DECODE	ss3694378015	Jul 13, 2019 (153)
27	PACBIO	ss3787324088	Jul 13, 2019 (153)
28	PACBIO	ss3792408849	Jul 13, 2019 (153)
29	PACBIO	ss3797291904	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3816245860	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3816245861	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3816245862	Jul 13, 2019 (153)
33	EVA	ss3833305444	Apr 27, 2020 (154)
34	EVA	ss3840224931	Apr 27, 2020 (154)
35	KOGIC	ss3972632137	Apr 27, 2020 (154)
36	KOGIC	ss3972632138	Apr 27, 2020 (154)
37	KOGIC	ss3972632139	Apr 27, 2020 (154)
38	KOGIC	ss3972632140	Apr 27, 2020 (154)
39	KOGIC	ss3972632141	Apr 27, 2020 (154)
40	GNOMAD	ss4258246596	Apr 26, 2021 (155)
41	GNOMAD	ss4258246597	Apr 26, 2021 (155)
42	GNOMAD	ss4258246598	Apr 26, 2021 (155)
43	GNOMAD	ss4258246599	Apr 26, 2021 (155)
44	GNOMAD	ss4258246600	Apr 26, 2021 (155)
45	GNOMAD	ss4258246602	Apr 26, 2021 (155)
46	GNOMAD	ss4258246603	Apr 26, 2021 (155)
47	GNOMAD	ss4258246604	Apr 26, 2021 (155)
48	GNOMAD	ss4258246605	Apr 26, 2021 (155)
49	GNOMAD	ss4258246606	Apr 26, 2021 (155)
50	GNOMAD	ss4258246607	Apr 26, 2021 (155)
51	GNOMAD	ss4258246608	Apr 26, 2021 (155)
52	GNOMAD	ss4258246609	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5207966087	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5207966088	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5207966089	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5207966090	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5207966091	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5207966092	Apr 26, 2021 (155)
59	1000G_HIGH_COVERAGE	ss5292080257	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5486698567	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5486698568	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5486698569	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5486698570	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5486698571	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5486698572	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5758228187	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5758228188	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5758228189	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5758228190	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5758228191	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5758228192	Oct 16, 2022 (156)
72	EVA	ss5838454230	Oct 16, 2022 (156)
73	EVA	ss5838454231	Oct 16, 2022 (156)
74	EVA	ss5905842771	Oct 16, 2022 (156)
75	1000Genomes	NC_000012.11 - 104882519	Oct 12, 2018 (152)
76	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 104882519	Oct 12, 2018 (152)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418056234 (NC_000012.12:104488740::GT 8387/134202) Row 418056235 (NC_000012.12:104488740::GTGT 7233/134186) Row 418056236 (NC_000012.12:104488740::GTGTGT 1803/134294)...	-	Apr 26, 2021 (155)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 29010138 (NC_000012.12:104488754:GTGT: 852/1832) Row 29010139 (NC_000012.12:104488756:GT: 824/1832) Row 29010140 (NC_000012.12:104488752:GTGTGT: 99/1832)...	-	Apr 27, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 29010138 (NC_000012.12:104488754:GTGT: 852/1832) Row 29010139 (NC_000012.12:104488756:GT: 824/1832) Row 29010140 (NC_000012.12:104488752:GTGTGT: 99/1832)...	-	Apr 27, 2020 (154)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 29010138 (NC_000012.12:104488754:GTGT: 852/1832) Row 29010139 (NC_000012.12:104488756:GT: 824/1832) Row 29010140 (NC_000012.12:104488752:GTGTGT: 99/1832)...	-	Apr 27, 2020 (154)
93	Korean Genome Project Submission ignored due to conflicting rows: Row 29010138 (NC_000012.12:104488754:GTGT: 852/1832) Row 29010139 (NC_000012.12:104488756:GT: 824/1832) Row 29010140 (NC_000012.12:104488752:GTGTGT: 99/1832)...	-	Apr 27, 2020 (154)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 29010138 (NC_000012.12:104488754:GTGT: 852/1832) Row 29010139 (NC_000012.12:104488756:GT: 824/1832) Row 29010140 (NC_000012.12:104488752:GTGTGT: 99/1832)...	-	Apr 27, 2020 (154)
95	8.3KJPN Submission ignored due to conflicting rows: Row 65935394 (NC_000012.11:104882518:GTGT: 7075/16756) Row 65935395 (NC_000012.11:104882518:GT: 8648/16756) Row 65935396 (NC_000012.11:104882518:GTGTGT: 202/16756)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 65935394 (NC_000012.11:104882518:GTGT: 7075/16756) Row 65935395 (NC_000012.11:104882518:GT: 8648/16756) Row 65935396 (NC_000012.11:104882518:GTGTGT: 202/16756)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 65935394 (NC_000012.11:104882518:GTGT: 7075/16756) Row 65935395 (NC_000012.11:104882518:GT: 8648/16756) Row 65935396 (NC_000012.11:104882518:GTGTGT: 202/16756)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 65935394 (NC_000012.11:104882518:GTGT: 7075/16756) Row 65935395 (NC_000012.11:104882518:GT: 8648/16756) Row 65935396 (NC_000012.11:104882518:GTGTGT: 202/16756)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 65935394 (NC_000012.11:104882518:GTGT: 7075/16756) Row 65935395 (NC_000012.11:104882518:GT: 8648/16756) Row 65935396 (NC_000012.11:104882518:GTGTGT: 202/16756)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 65935394 (NC_000012.11:104882518:GTGT: 7075/16756) Row 65935395 (NC_000012.11:104882518:GT: 8648/16756) Row 65935396 (NC_000012.11:104882518:GTGTGT: 202/16756)...	-	Apr 26, 2021 (155)
101	14KJPN Submission ignored due to conflicting rows: Row 92065291 (NC_000012.12:104488740:GTGT: 11387/27412) Row 92065292 (NC_000012.12:104488740:GT: 13916/27412) Row 92065293 (NC_000012.12:104488740::GT 46/27412)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 92065291 (NC_000012.12:104488740:GTGT: 11387/27412) Row 92065292 (NC_000012.12:104488740:GT: 13916/27412) Row 92065293 (NC_000012.12:104488740::GT 46/27412)...	-	Oct 16, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 92065291 (NC_000012.12:104488740:GTGT: 11387/27412) Row 92065292 (NC_000012.12:104488740:GT: 13916/27412) Row 92065293 (NC_000012.12:104488740::GT 46/27412)...	-	Oct 16, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 92065291 (NC_000012.12:104488740:GTGT: 11387/27412) Row 92065292 (NC_000012.12:104488740:GT: 13916/27412) Row 92065293 (NC_000012.12:104488740::GT 46/27412)...	-	Oct 16, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 92065291 (NC_000012.12:104488740:GTGT: 11387/27412) Row 92065292 (NC_000012.12:104488740:GT: 13916/27412) Row 92065293 (NC_000012.12:104488740::GT 46/27412)...	-	Oct 16, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 92065291 (NC_000012.12:104488740:GTGT: 11387/27412) Row 92065292 (NC_000012.12:104488740:GT: 13916/27412) Row 92065293 (NC_000012.12:104488740::GT 46/27412)...	-	Oct 16, 2022 (156)
107	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32911004 (NC_000012.11:104882520:GT: 1813/3708) Row 32911005 (NC_000012.11:104882518:GTGT: 1055/3708)	-	Apr 27, 2020 (154)
108	UK 10K study - Twins	-	Oct 12, 2018 (152)
109	ALFA	NC_000012.12 - 104488741	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)
rs141800360	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT	(self)
ss3972632141, ss4258246609	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT	(self)
ss4258246608	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT	(self)
ss4258246607, ss5905842771	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT	(self)
ss5207966091	NC_000012.11:104882518:GTGTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246606, ss5758228192	NC_000012.12:104488740:GTGTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT	(self)
ss3010277251, ss5207966092	NC_000012.11:104882518:GTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3694378015, ss4258246605, ss5758228191	NC_000012.12:104488740:GTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3972632140	NC_000012.12:104488750:GTGTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5207966089	NC_000012.11:104882518:GTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246604, ss5292080257, ss5486698572, ss5758228190	NC_000012.12:104488740:GTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3694378014	NC_000012.12:104488742:GTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3972632139	NC_000012.12:104488752:GTGTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss289149913	NC_000012.10:103406648:GTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
32911005, ss1707607398, ss1707607694, ss5207966087, ss5838454231	NC_000012.11:104882518:GTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816245862, ss4258246603, ss5486698567, ss5758228187	NC_000012.12:104488740:GTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3694378013	NC_000012.12:104488744:GTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3972632137	NC_000012.12:104488754:GTGT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss77883639	NC_000012.9:103385015:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss289149912, ss327574901	NC_000012.10:103406648:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
59267632, ss666582591, ss1372557880, ss1536741105, ss3787324088, ss3792408849, ss3797291904, ss3833305444, ss3840224931, ss5207966088, ss5838454230	NC_000012.11:104882518:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1710577654, ss1710577669	NC_000012.11:104882520:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3063744109, ss3063744110, ss3064574247, ss3064574248, ss3065495452, ss3065495453, ss3065495454, ss3816245861, ss4258246602, ss5486698568, ss5758228188	NC_000012.12:104488740:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816245860	NC_000012.12:104488742:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3694378012	NC_000012.12:104488746:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3972632138	NC_000012.12:104488756:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss95606503	NT_029419.12:67025854:GT:	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5207966090	NC_000012.11:104882518::GT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246596, ss5486698571, ss5758228189	NC_000012.12:104488740::GT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3694378011	NC_000012.12:104488748::GT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246597, ss5486698569	NC_000012.12:104488740::GTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3694378010	NC_000012.12:104488748::GTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246598, ss5486698570	NC_000012.12:104488740::GTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246599	NC_000012.12:104488740::GTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4258246600	NC_000012.12:104488740::GTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4225263424	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3180517270	NC_000012.12:104488740::GTGTGTGTGT… NC_000012.12:104488740::GTGTGTGTGTGT	NC_000012.12:104488740:GTGTGTGTGTG… NC_000012.12:104488740:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT

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

No publications for rs56383997

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs56383997