Name: rs9278766
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.

rs9278766

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:30786337-30786354 (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(T)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₂ / dup(T)₁₃ / ins(T)₂₂ / ins(T)₂₃ / ins(T)₃₉
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.3012 (1555/5162, ALFA)
(T)₁₈=0.1276 (639/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HCG20 : 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	5162	TTTTTTTTTTTTTTTTTT=0.5728	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.1077, TTTTTTTTTTTTTTTT=0.0155, TTTTTTTTTTTTTTTTT=0.3012, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTT=0.0000	0.547966	0.196886	0.255148	32
European	Sub	4860	TTTTTTTTTTTTTTTTTT=0.5473	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.1138, TTTTTTTTTTTTTTTT=0.0163, TTTTTTTTTTTTTTTTT=0.3198, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTT=0.0000	0.511666	0.212697	0.275638	32
African	Sub	160	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	156	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	14	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	82	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	34	TTTTTTTTTTTTTTTTTT=0.85	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5162	(T)₁₈=0.5728	del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.1077, delTT=0.0155, delT=0.3012, dupT=0.0000, dup(T)₁₂=0.0008, ins(T)₂₂=0.0008, ins(T)₂₃=0.0012
Allele Frequency Aggregator	European	Sub	4860	(T)₁₈=0.5473	del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.1138, delTT=0.0163, delT=0.3198, dupT=0.0000, dup(T)₁₂=0.0008, ins(T)₂₂=0.0008, ins(T)₂₃=0.0012
Allele Frequency Aggregator	African	Sub	160	(T)₁₈=1.000	del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dup(T)₁₂=0.000, ins(T)₂₂=0.000, ins(T)₂₃=0.000
Allele Frequency Aggregator	Latin American 2	Sub	82	(T)₁₈=1.00	del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₁₂=0.00, ins(T)₂₂=0.00, ins(T)₂₃=0.00
Allele Frequency Aggregator	Other	Sub	34	(T)₁₈=0.85	del(T)₇=0.00, del(T)₄=0.00, delTTT=0.09, delTT=0.03, delT=0.03, dupT=0.00, dup(T)₁₂=0.00, ins(T)₂₂=0.00, ins(T)₂₃=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(T)₁₈=1.00	del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₁₂=0.00, ins(T)₂₂=0.00, ins(T)₂₃=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(T)₁₈=1.0	del(T)₇=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₁₂=0.0, ins(T)₂₂=0.0, ins(T)₂₃=0.0
Allele Frequency Aggregator	Asian	Sub	4	(T)₁₈=1.0	del(T)₇=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₁₂=0.0, ins(T)₂₂=0.0, ins(T)₂₃=0.0
1000Genomes	Global	Study-wide	5008	(T)₁₈=0.1276	delT=0.8724
1000Genomes	African	Sub	1322	(T)₁₈=0.1899	delT=0.8101
1000Genomes	East Asian	Sub	1008	(T)₁₈=0.0605	delT=0.9395
1000Genomes	Europe	Sub	1006	(T)₁₈=0.1720	delT=0.8280
1000Genomes	South Asian	Sub	978	(T)₁₈=0.047	delT=0.953
1000Genomes	American	Sub	694	(T)₁₈=0.156	delT=0.844

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.30786348_30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786349_30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786350_30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786351_30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786352_30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786353_30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786354del
GRCh38.p14 chr 6	NC_000006.12:g.30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786353_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786352_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786351_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786350_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786349_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786348_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786347_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786346_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786343_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786342_30786354dup
GRCh38.p14 chr 6	NC_000006.12:g.30786354_30786355insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.30786354_30786355insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.30786354_30786355insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.30754125_30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754126_30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754127_30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754128_30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754129_30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754130_30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754131del
GRCh37.p13 chr 6	NC_000006.11:g.30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754130_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754129_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754128_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754127_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754126_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754125_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754124_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754123_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754120_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754119_30754131dup
GRCh37.p13 chr 6	NC_000006.11:g.30754131_30754132insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.30754131_30754132insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.30754131_30754132insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266061_2266066del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266062_2266066del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266063_2266066del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266064_2266066del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266065_2266066del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266066del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266065_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266064_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266063_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266062_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266061_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266060_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266059_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266058_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266057_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266054_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266053_2266066dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266066_2266067insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266066_2266067insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266066_2266067insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041432_2041437del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041433_2041437del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041434_2041437del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041435_2041437del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041436_2041437del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041437del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041436_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041435_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041434_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041433_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041432_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041431_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041430_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041429_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041428_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041425_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041424_2041437dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041437_2041438insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041437_2041438insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041437_2041438insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096590_2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096591_2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096592_2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096593_2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096594_2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096595_2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096596del
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096595_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096594_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096593_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096592_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096591_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096590_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096589_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096588_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096585_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096584_2096596dup
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096596_2096597insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096596_2096597insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096596_2096597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102210_2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102211_2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102212_2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102213_2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102214_2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102215_2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102216del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102215_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102214_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102213_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102212_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102211_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102210_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102209_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102208_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102205_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102204_2102216dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102216_2102217insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102216_2102217insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102216_2102217insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266167_2266172del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266168_2266172del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266169_2266172del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266170_2266172del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266171_2266172del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266172del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266171_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266170_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266169_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266168_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266167_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266166_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266165_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266164_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266163_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266160_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266159_2266172dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266172_2266173insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266172_2266173insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266172_2266173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047028_2047033del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047029_2047033del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047030_2047033del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047031_2047033del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047032_2047033del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047033del
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047032_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047031_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047030_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047029_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047028_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047027_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047026_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047025_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047024_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047021_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047020_2047033dup
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047033_2047034insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047033_2047034insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047033_2047034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: HCG20, HLA complex group 20 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HCG20 transcript	NR_138037.1: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	(T)₁₈=	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₂	dup(T)₁₃	ins(T)₂₂	ins(T)₂₃	ins(T)₃₉
GRCh38.p14 chr 6	NC_000006.12:g.30786337_30786354=	NC_000006.12:g.30786348_30786354del	NC_000006.12:g.30786349_30786354del	NC_000006.12:g.30786350_30786354del	NC_000006.12:g.30786351_30786354del	NC_000006.12:g.30786352_30786354del	NC_000006.12:g.30786353_30786354del	NC_000006.12:g.30786354del	NC_000006.12:g.30786354dup	NC_000006.12:g.30786353_30786354dup	NC_000006.12:g.30786352_30786354dup	NC_000006.12:g.30786351_30786354dup	NC_000006.12:g.30786350_30786354dup	NC_000006.12:g.30786349_30786354dup	NC_000006.12:g.30786348_30786354dup	NC_000006.12:g.30786347_30786354dup	NC_000006.12:g.30786346_30786354dup	NC_000006.12:g.30786343_30786354dup	NC_000006.12:g.30786342_30786354dup	NC_000006.12:g.30786354_30786355insTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.30786354_30786355insTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.30786354_30786355insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.30754114_30754131=	NC_000006.11:g.30754125_30754131del	NC_000006.11:g.30754126_30754131del	NC_000006.11:g.30754127_30754131del	NC_000006.11:g.30754128_30754131del	NC_000006.11:g.30754129_30754131del	NC_000006.11:g.30754130_30754131del	NC_000006.11:g.30754131del	NC_000006.11:g.30754131dup	NC_000006.11:g.30754130_30754131dup	NC_000006.11:g.30754129_30754131dup	NC_000006.11:g.30754128_30754131dup	NC_000006.11:g.30754127_30754131dup	NC_000006.11:g.30754126_30754131dup	NC_000006.11:g.30754125_30754131dup	NC_000006.11:g.30754124_30754131dup	NC_000006.11:g.30754123_30754131dup	NC_000006.11:g.30754120_30754131dup	NC_000006.11:g.30754119_30754131dup	NC_000006.11:g.30754131_30754132insTTTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.30754131_30754132insTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.30754131_30754132insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2266066dup	NT_113891.3:g.2266061_2266066del	NT_113891.3:g.2266062_2266066del	NT_113891.3:g.2266063_2266066del	NT_113891.3:g.2266064_2266066del	NT_113891.3:g.2266065_2266066del	NT_113891.3:g.2266066del	NT_113891.3:g.2266050_2266066=	NT_113891.3:g.2266065_2266066dup	NT_113891.3:g.2266064_2266066dup	NT_113891.3:g.2266063_2266066dup	NT_113891.3:g.2266062_2266066dup	NT_113891.3:g.2266061_2266066dup	NT_113891.3:g.2266060_2266066dup	NT_113891.3:g.2266059_2266066dup	NT_113891.3:g.2266058_2266066dup	NT_113891.3:g.2266057_2266066dup	NT_113891.3:g.2266054_2266066dup	NT_113891.3:g.2266053_2266066dup	NT_113891.3:g.2266066_2266067insTTTTTTTTTTTTTTTTTTTTTTT	NT_113891.3:g.2266066_2266067insTTTTTTTTTTTTTTTTTTTTTTTT	NT_113891.3:g.2266066_2266067insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2041437dup	NT_167248.2:g.2041432_2041437del	NT_167248.2:g.2041433_2041437del	NT_167248.2:g.2041434_2041437del	NT_167248.2:g.2041435_2041437del	NT_167248.2:g.2041436_2041437del	NT_167248.2:g.2041437del	NT_167248.2:g.2041421_2041437=	NT_167248.2:g.2041436_2041437dup	NT_167248.2:g.2041435_2041437dup	NT_167248.2:g.2041434_2041437dup	NT_167248.2:g.2041433_2041437dup	NT_167248.2:g.2041432_2041437dup	NT_167248.2:g.2041431_2041437dup	NT_167248.2:g.2041430_2041437dup	NT_167248.2:g.2041429_2041437dup	NT_167248.2:g.2041428_2041437dup	NT_167248.2:g.2041425_2041437dup	NT_167248.2:g.2041424_2041437dup	NT_167248.2:g.2041437_2041438insTTTTTTTTTTTTTTTTTTTTTTT	NT_167248.2:g.2041437_2041438insTTTTTTTTTTTTTTTTTTTTTTTT	NT_167248.2:g.2041437_2041438insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2096579_2096596=	NT_167246.2:g.2096590_2096596del	NT_167246.2:g.2096591_2096596del	NT_167246.2:g.2096592_2096596del	NT_167246.2:g.2096593_2096596del	NT_167246.2:g.2096594_2096596del	NT_167246.2:g.2096595_2096596del	NT_167246.2:g.2096596del	NT_167246.2:g.2096596dup	NT_167246.2:g.2096595_2096596dup	NT_167246.2:g.2096594_2096596dup	NT_167246.2:g.2096593_2096596dup	NT_167246.2:g.2096592_2096596dup	NT_167246.2:g.2096591_2096596dup	NT_167246.2:g.2096590_2096596dup	NT_167246.2:g.2096589_2096596dup	NT_167246.2:g.2096588_2096596dup	NT_167246.2:g.2096585_2096596dup	NT_167246.2:g.2096584_2096596dup	NT_167246.2:g.2096596_2096597insTTTTTTTTTTTTTTTTTTTTTT	NT_167246.2:g.2096596_2096597insTTTTTTTTTTTTTTTTTTTTTTT	NT_167246.2:g.2096596_2096597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2102199_2102216=	NT_167246.1:g.2102210_2102216del	NT_167246.1:g.2102211_2102216del	NT_167246.1:g.2102212_2102216del	NT_167246.1:g.2102213_2102216del	NT_167246.1:g.2102214_2102216del	NT_167246.1:g.2102215_2102216del	NT_167246.1:g.2102216del	NT_167246.1:g.2102216dup	NT_167246.1:g.2102215_2102216dup	NT_167246.1:g.2102214_2102216dup	NT_167246.1:g.2102213_2102216dup	NT_167246.1:g.2102212_2102216dup	NT_167246.1:g.2102211_2102216dup	NT_167246.1:g.2102210_2102216dup	NT_167246.1:g.2102209_2102216dup	NT_167246.1:g.2102208_2102216dup	NT_167246.1:g.2102205_2102216dup	NT_167246.1:g.2102204_2102216dup	NT_167246.1:g.2102216_2102217insTTTTTTTTTTTTTTTTTTTTTT	NT_167246.1:g.2102216_2102217insTTTTTTTTTTTTTTTTTTTTTTT	NT_167246.1:g.2102216_2102217insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2266172dup	NT_113891.2:g.2266167_2266172del	NT_113891.2:g.2266168_2266172del	NT_113891.2:g.2266169_2266172del	NT_113891.2:g.2266170_2266172del	NT_113891.2:g.2266171_2266172del	NT_113891.2:g.2266172del	NT_113891.2:g.2266156_2266172=	NT_113891.2:g.2266171_2266172dup	NT_113891.2:g.2266170_2266172dup	NT_113891.2:g.2266169_2266172dup	NT_113891.2:g.2266168_2266172dup	NT_113891.2:g.2266167_2266172dup	NT_113891.2:g.2266166_2266172dup	NT_113891.2:g.2266165_2266172dup	NT_113891.2:g.2266164_2266172dup	NT_113891.2:g.2266163_2266172dup	NT_113891.2:g.2266160_2266172dup	NT_113891.2:g.2266159_2266172dup	NT_113891.2:g.2266172_2266173insTTTTTTTTTTTTTTTTTTTTTTT	NT_113891.2:g.2266172_2266173insTTTTTTTTTTTTTTTTTTTTTTTT	NT_113891.2:g.2266172_2266173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2047033dup	NT_167248.1:g.2047028_2047033del	NT_167248.1:g.2047029_2047033del	NT_167248.1:g.2047030_2047033del	NT_167248.1:g.2047031_2047033del	NT_167248.1:g.2047032_2047033del	NT_167248.1:g.2047033del	NT_167248.1:g.2047017_2047033=	NT_167248.1:g.2047032_2047033dup	NT_167248.1:g.2047031_2047033dup	NT_167248.1:g.2047030_2047033dup	NT_167248.1:g.2047029_2047033dup	NT_167248.1:g.2047028_2047033dup	NT_167248.1:g.2047027_2047033dup	NT_167248.1:g.2047026_2047033dup	NT_167248.1:g.2047025_2047033dup	NT_167248.1:g.2047024_2047033dup	NT_167248.1:g.2047021_2047033dup	NT_167248.1:g.2047020_2047033dup	NT_167248.1:g.2047033_2047034insTTTTTTTTTTTTTTTTTTTTTTT	NT_167248.1:g.2047033_2047034insTTTTTTTTTTTTTTTTTTTTTTTT	NT_167248.1:g.2047033_2047034insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79848689	Aug 21, 2014 (144)
2	HGSV	ss81604750	Aug 21, 2014 (142)
3	HUMANGENOME_JCVI	ss95424065	Feb 06, 2009 (130)
4	BUSHMAN	ss193853835	Jul 04, 2010 (137)
5	GMI	ss288693151	May 04, 2012 (137)
6	PJP	ss295272689	May 09, 2011 (137)
7	SSMP	ss663686959	Apr 01, 2015 (144)
8	1000GENOMES	ss1375318387	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1705102399	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1705103584	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710261793	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710261794	Jan 10, 2018 (151)
13	EVA_UK10K_ALSPAC	ss1710261795	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1710261797	Jan 10, 2018 (151)
15	SYSTEMSBIOZJU	ss2626301344	Nov 08, 2017 (151)
16	SWEGEN	ss2998774745	Nov 08, 2017 (151)
17	URBANLAB	ss3648305559	Oct 12, 2018 (152)
18	KHV_HUMAN_GENOMES	ss3807960660	Jul 13, 2019 (153)
19	EVA	ss3829820796	Apr 26, 2020 (154)
20	GNOMAD	ss4139284256	Apr 26, 2021 (155)
21	GNOMAD	ss4139284257	Apr 26, 2021 (155)
22	GNOMAD	ss4139284258	Apr 26, 2021 (155)
23	GNOMAD	ss4139284259	Apr 26, 2021 (155)
24	GNOMAD	ss4139284260	Apr 26, 2021 (155)
25	GNOMAD	ss4139284261	Apr 26, 2021 (155)
26	GNOMAD	ss4139284262	Apr 26, 2021 (155)
27	GNOMAD	ss4139284263	Apr 26, 2021 (155)
28	GNOMAD	ss4139284264	Apr 26, 2021 (155)
29	GNOMAD	ss4139284265	Apr 26, 2021 (155)
30	GNOMAD	ss4139284266	Apr 26, 2021 (155)
31	GNOMAD	ss4139284267	Apr 26, 2021 (155)
32	GNOMAD	ss4139284268	Apr 26, 2021 (155)
33	GNOMAD	ss4139284270	Apr 26, 2021 (155)
34	GNOMAD	ss4139284271	Apr 26, 2021 (155)
35	GNOMAD	ss4139284272	Apr 26, 2021 (155)
36	GNOMAD	ss4139284273	Apr 26, 2021 (155)
37	GNOMAD	ss4139284274	Apr 26, 2021 (155)
38	GNOMAD	ss4139284275	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5176801546	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5176801547	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5176801548	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5267908749	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5267908750	Oct 13, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5267908751	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5465648277	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5465648278	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5465648279	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5714647258	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5714647259	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5714647260	Oct 13, 2022 (156)
51	1000Genomes	NC_000006.11 - 30754114	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17448874 (NC_000006.11:30754113:TTT: 960/3854) Row 17448876 (NC_000006.11:30754114:T: 316/3854)	-	Oct 12, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 17448874 (NC_000006.11:30754113:TTT: 960/3854) Row 17448876 (NC_000006.11:30754114:T: 316/3854)	-	Oct 12, 2018 (152)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221066035 (NC_000006.12:30786336::T 24/112192) Row 221066036 (NC_000006.12:30786336::TT 1/112198) Row 221066037 (NC_000006.12:30786336::TTT 2/112200)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 34770853 (NC_000006.11:30754113:TTT: 2579/16584) Row 34770854 (NC_000006.11:30754113:T: 3460/16584) Row 34770855 (NC_000006.11:30754113:TTTT: 3/16584)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 34770853 (NC_000006.11:30754113:TTT: 2579/16584) Row 34770854 (NC_000006.11:30754113:T: 3460/16584) Row 34770855 (NC_000006.11:30754113:TTTT: 3/16584)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 34770853 (NC_000006.11:30754113:TTT: 2579/16584) Row 34770854 (NC_000006.11:30754113:T: 3460/16584) Row 34770855 (NC_000006.11:30754113:TTTT: 3/16584)	-	Apr 26, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 48484362 (NC_000006.12:30786336:TTT: 4178/24738) Row 48484363 (NC_000006.12:30786336:T: 4874/24738) Row 48484364 (NC_000006.12:30786336:TTTT: 4/24738)	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 48484362 (NC_000006.12:30786336:TTT: 4178/24738) Row 48484363 (NC_000006.12:30786336:T: 4874/24738) Row 48484364 (NC_000006.12:30786336:TTTT: 4/24738)	-	Oct 13, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 48484362 (NC_000006.12:30786336:TTT: 4178/24738) Row 48484363 (NC_000006.12:30786336:T: 4874/24738) Row 48484364 (NC_000006.12:30786336:TTTT: 4/24738)	-	Oct 13, 2022 (156)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17448874 (NC_000006.11:30754113:TTT: 993/3708) Row 17448876 (NC_000006.11:30754114:T: 240/3708)	-	Oct 12, 2018 (152)
80	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17448874 (NC_000006.11:30754113:TTT: 993/3708) Row 17448875 (NC_000006.11:30754115:T: 2199/3708) Row 17448876 (NC_000006.11:30754114:TT: 240/3708)	-	Apr 26, 2020 (154)
81	UK 10K study - Twins Submission ignored due to conflicting rows: Row 17448874 (NC_000006.11:30754113:TTT: 993/3708) Row 17448876 (NC_000006.11:30754114:T: 240/3708)	-	Oct 12, 2018 (152)
82	ALFA	NC_000006.12 - 30786337	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)
rs147244428	May 04, 2012 (137)
rs202177882	Jul 30, 2012 (137)
rs556595787	Jul 01, 2015 (144)
rs58952401	May 25, 2008 (130)
rs112949190	Jul 30, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4139284275	NC_000006.12:30786336:TTTTTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4139284274	NC_000006.12:30786336:TTTTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5176801548	NC_000006.11:30754113:TTTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4139284273, ss5714647260	NC_000006.12:30786336:TTTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss79848689	NC_000006.9:30862107:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss288693151	NC_000006.10:30862092:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss295272689	NC_000006.10:30862107:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1705102399, ss1705103584, ss2626301344, ss2998774745, ss3829820796, ss5176801546	NC_000006.11:30754113:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3648305559, ss4139284272, ss5267908750, ss5465648279, ss5714647258	NC_000006.12:30786336:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss193853835	NT_007592.15:30694113:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss95424065	NT_007592.15:30694128:TTT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1710261794, ss1710261797	NC_000006.11:30754114:TT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4139284271, ss5267908751, ss5465648277	NC_000006.12:30786336:TT:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss81604750	NC_000006.9:30862109:T:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
31295444, ss663686959, ss1375318387, ss5176801547	NC_000006.11:30754113:T:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
	NC_000006.11:30754114:T:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss1710261793, ss1710261795	NC_000006.11:30754115:T:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3807960660, ss4139284270, ss5267908749, ss5465648278, ss5714647259	NC_000006.12:30786336:T:	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4139284256	NC_000006.12:30786336::T	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4139284257	NC_000006.12:30786336::TT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4139284258	NC_000006.12:30786336::TTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284259	NC_000006.12:30786336::TTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284260	NC_000006.12:30786336::TTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284261	NC_000006.12:30786336::TTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284262	NC_000006.12:30786336::TTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284263	NC_000006.12:30786336::TTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284264	NC_000006.12:30786336::TTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284265	NC_000006.12:30786336::TTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284266	NC_000006.12:30786336::TTTTTTTTTTT… NC_000006.12:30786336::TTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284267	NC_000006.12:30786336::TTTTTTTTTTT… NC_000006.12:30786336::TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10756670792	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4139284268	NC_000006.12:30786336::TTTTTTTTTTT… NC_000006.12:30786336::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:30786336:TTTTTTTTTTTT… NC_000006.12:30786336:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs9278766

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

rs9278766