Name: rs61221276
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.

rs61221276

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:271025-271044 (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)₁₁ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / 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)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.2992 (1625/5432, ALFA)
(T)₂₀=0.00 (0/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PDCD6-DT : Intron Variant
PDCD6 : 2KB Upstream Variant
PDCD6-AHRR : 2KB Upstream Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	5432	TTTTTTTTTTTTTTTTTTTT=0.6285	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0311, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0169, TTTTTTTTTTTTTTTTTTTTTT=0.2992, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0041, TTTTTTTTTTTTTTTTTTTTTTT=0.0184, TTTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.62774	0.235245	0.137015	32
European	Sub	5050	TTTTTTTTTTTTTTTTTTTT=0.6012	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0335, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0182, TTTTTTTTTTTTTTTTTTTTTT=0.3214, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0044, TTTTTTTTTTTTTTTTTTTTTTT=0.0194, TTTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.595784	0.25527	0.148946	32
African	Sub	150	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	146	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	54	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	94	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	54	TTTTTTTTTTTTTTTTTTTT=0.93	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.961538	0.038462	0.0	14

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	5432	(T)₂₀=0.6285	del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0311, delT=0.0000, dupT=0.0169, dupTT=0.2992, dupTTT=0.0184, dup(T)₄=0.0018, dup(T)₅=0.0000, dup(T)₆=0.0041
Allele Frequency Aggregator	European	Sub	5050	(T)₂₀=0.6012	del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0335, delT=0.0000, dupT=0.0182, dupTT=0.3214, dupTTT=0.0194, dup(T)₄=0.0020, dup(T)₅=0.0000, dup(T)₆=0.0044
Allele Frequency Aggregator	African	Sub	150	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	94	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Other	Sub	54	(T)₂₀=0.93	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.04, dupTTT=0.04, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	54	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dup(T)₁₁=1.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 5	NC_000005.10:g.271034_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271035_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271036_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271037_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271038_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271039_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271040_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271041_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271042_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271043_271044del
GRCh38.p14 chr 5	NC_000005.10:g.271044del
GRCh38.p14 chr 5	NC_000005.10:g.271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271043_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271042_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271041_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271040_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271039_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271038_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271037_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271036_271044dup
GRCh38.p14 chr 5	NC_000005.10:g.271034_271044dup
GRCh37.p13 chr 5	NC_000005.9:g.271149_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271150_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271151_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271152_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271153_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271154_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271155_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271156_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271157_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271158_271159del
GRCh37.p13 chr 5	NC_000005.9:g.271159del
GRCh37.p13 chr 5	NC_000005.9:g.271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271158_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271157_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271156_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271155_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271154_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271153_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271152_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271151_271159dup
GRCh37.p13 chr 5	NC_000005.9:g.271149_271159dup

Gene: PDCD6, programmed cell death 6 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PDCD6 transcript variant 2	NM_001267556.2:c.	N/A	Upstream Transcript Variant
PDCD6 transcript variant 3	NM_001267557.2:c.	N/A	Upstream Transcript Variant
PDCD6 transcript variant 4	NM_001267558.2:c.	N/A	Upstream Transcript Variant
PDCD6 transcript variant 5	NM_001267559.2:c.	N/A	Upstream Transcript Variant
PDCD6 transcript variant 1	NM_013232.4:c.	N/A	Upstream Transcript Variant
PDCD6 transcript variant 6	NR_073609.2:n.	N/A	Upstream Transcript Variant

Gene: PDCD6-DT, PDCD6 divergent transcript (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PDCD6-DT transcript	NR_104613.1:n.	N/A	Intron Variant

Gene: PDCD6-AHRR, PDCD6-AHRR readthrough (NMD candidate) (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PDCD6-AHRR transcript variant 1	NR_165159.2:n.	N/A	Upstream Transcript Variant
PDCD6-AHRR transcript variant 2	NR_165163.2:n.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₀=	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	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)₁₁
GRCh38.p14 chr 5	NC_000005.10:g.271025_271044=	NC_000005.10:g.271034_271044del	NC_000005.10:g.271035_271044del	NC_000005.10:g.271036_271044del	NC_000005.10:g.271037_271044del	NC_000005.10:g.271038_271044del	NC_000005.10:g.271039_271044del	NC_000005.10:g.271040_271044del	NC_000005.10:g.271041_271044del	NC_000005.10:g.271042_271044del	NC_000005.10:g.271043_271044del	NC_000005.10:g.271044del	NC_000005.10:g.271044dup	NC_000005.10:g.271043_271044dup	NC_000005.10:g.271042_271044dup	NC_000005.10:g.271041_271044dup	NC_000005.10:g.271040_271044dup	NC_000005.10:g.271039_271044dup	NC_000005.10:g.271038_271044dup	NC_000005.10:g.271037_271044dup	NC_000005.10:g.271036_271044dup	NC_000005.10:g.271034_271044dup
GRCh37.p13 chr 5	NC_000005.9:g.271140_271159=	NC_000005.9:g.271149_271159del	NC_000005.9:g.271150_271159del	NC_000005.9:g.271151_271159del	NC_000005.9:g.271152_271159del	NC_000005.9:g.271153_271159del	NC_000005.9:g.271154_271159del	NC_000005.9:g.271155_271159del	NC_000005.9:g.271156_271159del	NC_000005.9:g.271157_271159del	NC_000005.9:g.271158_271159del	NC_000005.9:g.271159del	NC_000005.9:g.271159dup	NC_000005.9:g.271158_271159dup	NC_000005.9:g.271157_271159dup	NC_000005.9:g.271156_271159dup	NC_000005.9:g.271155_271159dup	NC_000005.9:g.271154_271159dup	NC_000005.9:g.271153_271159dup	NC_000005.9:g.271152_271159dup	NC_000005.9:g.271151_271159dup	NC_000005.9:g.271149_271159dup

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#.

61 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83155061	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95383702	Feb 13, 2009 (137)
3	PJP	ss295208988	May 09, 2011 (137)
4	EVA_GENOME_DK	ss1583574597	Apr 01, 2015 (144)
5	SWEGEN	ss2996295897	Nov 08, 2017 (151)
6	URBANLAB	ss3647963017	Oct 12, 2018 (152)
7	EVA_DECODE	ss3713933024	Jul 13, 2019 (153)
8	EVA_DECODE	ss3713933025	Jul 13, 2019 (153)
9	EVA_DECODE	ss3713933026	Jul 13, 2019 (153)
10	EVA_DECODE	ss3713933027	Jul 13, 2019 (153)
11	EVA_DECODE	ss3713933028	Jul 13, 2019 (153)
12	PACBIO	ss3784996329	Jul 13, 2019 (153)
13	PACBIO	ss3790416441	Jul 13, 2019 (153)
14	PACBIO	ss3790416442	Jul 13, 2019 (153)
15	PACBIO	ss3790416443	Jul 13, 2019 (153)
16	PACBIO	ss3795292907	Jul 13, 2019 (153)
17	PACBIO	ss3795292908	Jul 13, 2019 (153)
18	PACBIO	ss3795292909	Jul 13, 2019 (153)
19	EVA	ss3829047394	Apr 26, 2020 (154)
20	GNOMAD	ss4097922029	Apr 26, 2021 (155)
21	GNOMAD	ss4097922030	Apr 26, 2021 (155)
22	GNOMAD	ss4097922031	Apr 26, 2021 (155)
23	GNOMAD	ss4097922032	Apr 26, 2021 (155)
24	GNOMAD	ss4097922033	Apr 26, 2021 (155)
25	GNOMAD	ss4097922034	Apr 26, 2021 (155)
26	GNOMAD	ss4097922035	Apr 26, 2021 (155)
27	GNOMAD	ss4097922036	Apr 26, 2021 (155)
28	GNOMAD	ss4097922037	Apr 26, 2021 (155)
29	GNOMAD	ss4097922038	Apr 26, 2021 (155)
30	GNOMAD	ss4097922039	Apr 26, 2021 (155)
31	GNOMAD	ss4097922040	Apr 26, 2021 (155)
32	GNOMAD	ss4097922041	Apr 26, 2021 (155)
33	GNOMAD	ss4097922042	Apr 26, 2021 (155)
34	GNOMAD	ss4097922043	Apr 26, 2021 (155)
35	GNOMAD	ss4097922044	Apr 26, 2021 (155)
36	GNOMAD	ss4097922045	Apr 26, 2021 (155)
37	GNOMAD	ss4097922046	Apr 26, 2021 (155)
38	GNOMAD	ss4097922047	Apr 26, 2021 (155)
39	GNOMAD	ss4097922048	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5169989670	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5169989671	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5169989672	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5169989673	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5169989674	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5262570290	Oct 13, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5262570291	Oct 13, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5262570292	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5262570293	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5262570294	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5262570295	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5460954776	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5460954777	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5460954778	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5460954779	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5460954780	Oct 13, 2022 (156)
56	HUGCELL_USP	ss5460954781	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5705548489	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5705548490	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5705548491	Oct 13, 2022 (156)
60	TOMMO_GENOMICS	ss5705548492	Oct 13, 2022 (156)
61	TOMMO_GENOMICS	ss5705548493	Oct 13, 2022 (156)
62	The Danish reference pan genome	NC_000005.9 - 271140	Apr 26, 2020 (154)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 177564520 (NC_000005.10:271024::T 4351/100246) Row 177564521 (NC_000005.10:271024::TT 41271/100076) Row 177564522 (NC_000005.10:271024::TTT 1699/100284)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 27958977 (NC_000005.9:271139:TT: 383/15906) Row 27958978 (NC_000005.9:271139::TT 2987/15906) Row 27958979 (NC_000005.9:271139::TTT 473/15906)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 27958977 (NC_000005.9:271139:TT: 383/15906) Row 27958978 (NC_000005.9:271139::TT 2987/15906) Row 27958979 (NC_000005.9:271139::TTT 473/15906)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 27958977 (NC_000005.9:271139:TT: 383/15906) Row 27958978 (NC_000005.9:271139::TT 2987/15906) Row 27958979 (NC_000005.9:271139::TTT 473/15906)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 27958977 (NC_000005.9:271139:TT: 383/15906) Row 27958978 (NC_000005.9:271139::TT 2987/15906) Row 27958979 (NC_000005.9:271139::TTT 473/15906)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 27958977 (NC_000005.9:271139:TT: 383/15906) Row 27958978 (NC_000005.9:271139::TT 2987/15906) Row 27958979 (NC_000005.9:271139::TTT 473/15906)...	-	Apr 26, 2021 (155)
88	14KJPN Submission ignored due to conflicting rows: Row 39385593 (NC_000005.10:271024::TT 5135/27446) Row 39385594 (NC_000005.10:271024:TT: 757/27446) Row 39385595 (NC_000005.10:271024:T: 221/27446)...	-	Oct 13, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 39385593 (NC_000005.10:271024::TT 5135/27446) Row 39385594 (NC_000005.10:271024:TT: 757/27446) Row 39385595 (NC_000005.10:271024:T: 221/27446)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 39385593 (NC_000005.10:271024::TT 5135/27446) Row 39385594 (NC_000005.10:271024:TT: 757/27446) Row 39385595 (NC_000005.10:271024:T: 221/27446)...	-	Oct 13, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 39385593 (NC_000005.10:271024::TT 5135/27446) Row 39385594 (NC_000005.10:271024:TT: 757/27446) Row 39385595 (NC_000005.10:271024:T: 221/27446)...	-	Oct 13, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 39385593 (NC_000005.10:271024::TT 5135/27446) Row 39385594 (NC_000005.10:271024:TT: 757/27446) Row 39385595 (NC_000005.10:271024:T: 221/27446)...	-	Oct 13, 2022 (156)
93	ALFA	NC_000005.10 - 271025	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)
rs70955222	May 11, 2012 (137)
rs146004341	May 04, 2012 (137)
rs796387128	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4097922048	NC_000005.10:271024:TTTTTTTTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4097922047	NC_000005.10:271024:TTTTTTTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4097922046	NC_000005.10:271024:TTTTTTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4097922045	NC_000005.10:271024:TTTTTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4097922044	NC_000005.10:271024:TTTTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4097922043	NC_000005.10:271024:TTTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4097922042	NC_000005.10:271024:TTTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4097922041, ss5262570293, ss5460954781	NC_000005.10:271024:TTTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss2996295897	NC_000005.9:271139:TTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4097922040, ss5262570294, ss5460954778	NC_000005.10:271024:TTT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss83155061	NC_000005.8:324157:TT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3784996329, ss3790416441, ss3795292907, ss5169989670	NC_000005.9:271139:TT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3713933024, ss4097922039, ss5262570292, ss5460954779, ss5705548490	NC_000005.10:271024:TT:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5169989674	NC_000005.9:271139:T:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4097922038, ss5262570295, ss5705548491	NC_000005.10:271024:T:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3713933025	NC_000005.10:271025:T:	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3790416442, ss3795292908, ss5169989673	NC_000005.9:271139::T	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922029, ss5262570291, ss5460954776, ss5705548492	NC_000005.10:271024::T	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3713933026	NC_000005.10:271026::T	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss295208988	NC_000005.8:324158::TT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3790416443, ss3795292909, ss3829047394, ss5169989671	NC_000005.9:271139::TT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3647963017, ss4097922030, ss5262570290, ss5460954777, ss5705548489	NC_000005.10:271024::TT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3713933027	NC_000005.10:271026::TT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss95383702	NT_006576.16:261159::TT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5169989672	NC_000005.9:271139::TTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922031, ss5460954780, ss5705548493	NC_000005.10:271024::TTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3713933028	NC_000005.10:271026::TTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922032	NC_000005.10:271024::TTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922033	NC_000005.10:271024::TTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922034	NC_000005.10:271024::TTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7509446823	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922035	NC_000005.10:271024::TTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922036	NC_000005.10:271024::TTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4097922037	NC_000005.10:271024::TTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
83907	NC_000005.9:271139::TTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1583574597	NC_000005.9:271144::TTTTTTTTTTT	NC_000005.10:271024:TTTTTTTTTTTTTT… NC_000005.10:271024:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs61221276

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

rs61221276