Name: rs781711813
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.

rs781711813

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:161220365-161220386 (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)₁₀ / del(T)₇ / del(T)₆ / del…
del(T)₁₀ / 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)₇ / dup(T)₁₀ / dup(T)₁₁ / ins(T)₂₆ / ins(T)₃₃ / ins(T)₃₈
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.0998 (965/9668, ALFA)
(T)₂₂=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	9668	TTTTTTTTTTTTTTTTTTTTTT=0.8948	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0998, TTTTTTTTTTTTTTTTTTTTTTTT=0.0053, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.84977	0.04743	0.1028	32
European	Sub	7570	TTTTTTTTTTTTTTTTTTTTTT=0.8661	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.1272, TTTTTTTTTTTTTTTTTTTTTTTT=0.0066, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.807919	0.060728	0.131354	32
African	Sub	1412	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	66	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1346	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	58	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	40	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	86	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	280	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	44	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	218	TTTTTTTTTTTTTTTTTTTTTT=0.986	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.009, TTTTTTTTTTTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.990741	0.0	0.009259	0

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	9668	(T)₂₂=0.8948	del(T)₁₀=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=0.0000, delT=0.0000, dupT=0.0998, dupTT=0.0053, dupTTT=0.0000, dup(T)₄=0.0000, ins(T)₃₃=0.0001
Allele Frequency Aggregator	European	Sub	7570	(T)₂₂=0.8661	del(T)₁₀=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=0.0000, delT=0.0000, dupT=0.1272, dupTT=0.0066, dupTTT=0.0000, dup(T)₄=0.0000, ins(T)₃₃=0.0001
Allele Frequency Aggregator	African	Sub	1412	(T)₂₂=1.0000	del(T)₁₀=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=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, ins(T)₃₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	280	(T)₂₂=1.000	del(T)₁₀=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, ins(T)₃₃=0.000
Allele Frequency Aggregator	Other	Sub	218	(T)₂₂=0.986	del(T)₁₀=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=0.009, dupTT=0.005, dupTTT=0.000, dup(T)₄=0.000, ins(T)₃₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	86	(T)₂₂=1.00	del(T)₁₀=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, ins(T)₃₃=0.00
Allele Frequency Aggregator	Asian	Sub	58	(T)₂₂=1.00	del(T)₁₀=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, ins(T)₃₃=0.00
Allele Frequency Aggregator	South Asian	Sub	44	(T)₂₂=1.00	del(T)₁₀=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, ins(T)₃₃=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTT=0.55

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 1	NC_000001.11:g.161220377_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220380_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220381_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220382_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220383_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220384_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220385_161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220386del
GRCh38.p14 chr 1	NC_000001.11:g.161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220385_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220384_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220383_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220382_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220380_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220377_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220376_161220386dup
GRCh38.p14 chr 1	NC_000001.11:g.161220386_161220387insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.161220386_161220387insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.161220386_161220387insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.161190167_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190170_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190171_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190172_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190173_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190174_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190175_161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190176del
GRCh37.p13 chr 1	NC_000001.10:g.161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190175_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190174_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190173_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190172_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190170_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190167_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190166_161190176dup
GRCh37.p13 chr 1	NC_000001.10:g.161190176_161190177insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.161190176_161190177insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.161190176_161190177insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
FCER1G RefSeqGene	NG_029043.1:g.10081_10090del
FCER1G RefSeqGene	NG_029043.1:g.10084_10090del
FCER1G RefSeqGene	NG_029043.1:g.10085_10090del
FCER1G RefSeqGene	NG_029043.1:g.10086_10090del
FCER1G RefSeqGene	NG_029043.1:g.10087_10090del
FCER1G RefSeqGene	NG_029043.1:g.10088_10090del
FCER1G RefSeqGene	NG_029043.1:g.10089_10090del
FCER1G RefSeqGene	NG_029043.1:g.10090del
FCER1G RefSeqGene	NG_029043.1:g.10090dup
FCER1G RefSeqGene	NG_029043.1:g.10089_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10088_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10087_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10086_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10084_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10081_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10080_10090dup
FCER1G RefSeqGene	NG_029043.1:g.10090_10091insTTTTTTTTTTTTTTTTTTTTTTTTTT
FCER1G RefSeqGene	NG_029043.1:g.10090_10091insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
FCER1G RefSeqGene	NG_029043.1:g.10090_10091insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
APOA2 RefSeqGene	NG_012043.1:g.8255_8264del
APOA2 RefSeqGene	NG_012043.1:g.8258_8264del
APOA2 RefSeqGene	NG_012043.1:g.8259_8264del
APOA2 RefSeqGene	NG_012043.1:g.8260_8264del
APOA2 RefSeqGene	NG_012043.1:g.8261_8264del
APOA2 RefSeqGene	NG_012043.1:g.8262_8264del
APOA2 RefSeqGene	NG_012043.1:g.8263_8264del
APOA2 RefSeqGene	NG_012043.1:g.8264del
APOA2 RefSeqGene	NG_012043.1:g.8264dup
APOA2 RefSeqGene	NG_012043.1:g.8263_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8262_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8261_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8260_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8258_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8255_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8254_8264dup
APOA2 RefSeqGene	NG_012043.1:g.8264_8265insAAAAAAAAAAAAAAAAAAAAAAAAAA
APOA2 RefSeqGene	NG_012043.1:g.8264_8265insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
APOA2 RefSeqGene	NG_012043.1:g.8264_8265insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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)₂₂=	del(T)₁₀	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)₇	dup(T)₁₀	dup(T)₁₁	ins(T)₂₆	ins(T)₃₃	ins(T)₃₈
GRCh38.p14 chr 1	NC_000001.11:g.161220365_161220386=	NC_000001.11:g.161220377_161220386del	NC_000001.11:g.161220380_161220386del	NC_000001.11:g.161220381_161220386del	NC_000001.11:g.161220382_161220386del	NC_000001.11:g.161220383_161220386del	NC_000001.11:g.161220384_161220386del	NC_000001.11:g.161220385_161220386del	NC_000001.11:g.161220386del	NC_000001.11:g.161220386dup	NC_000001.11:g.161220385_161220386dup	NC_000001.11:g.161220384_161220386dup	NC_000001.11:g.161220383_161220386dup	NC_000001.11:g.161220382_161220386dup	NC_000001.11:g.161220380_161220386dup	NC_000001.11:g.161220377_161220386dup	NC_000001.11:g.161220376_161220386dup	NC_000001.11:g.161220386_161220387insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.161220386_161220387insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.161220386_161220387insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.161190155_161190176=	NC_000001.10:g.161190167_161190176del	NC_000001.10:g.161190170_161190176del	NC_000001.10:g.161190171_161190176del	NC_000001.10:g.161190172_161190176del	NC_000001.10:g.161190173_161190176del	NC_000001.10:g.161190174_161190176del	NC_000001.10:g.161190175_161190176del	NC_000001.10:g.161190176del	NC_000001.10:g.161190176dup	NC_000001.10:g.161190175_161190176dup	NC_000001.10:g.161190174_161190176dup	NC_000001.10:g.161190173_161190176dup	NC_000001.10:g.161190172_161190176dup	NC_000001.10:g.161190170_161190176dup	NC_000001.10:g.161190167_161190176dup	NC_000001.10:g.161190166_161190176dup	NC_000001.10:g.161190176_161190177insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.161190176_161190177insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.161190176_161190177insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
FCER1G RefSeqGene	NG_029043.1:g.10069_10090=	NG_029043.1:g.10081_10090del	NG_029043.1:g.10084_10090del	NG_029043.1:g.10085_10090del	NG_029043.1:g.10086_10090del	NG_029043.1:g.10087_10090del	NG_029043.1:g.10088_10090del	NG_029043.1:g.10089_10090del	NG_029043.1:g.10090del	NG_029043.1:g.10090dup	NG_029043.1:g.10089_10090dup	NG_029043.1:g.10088_10090dup	NG_029043.1:g.10087_10090dup	NG_029043.1:g.10086_10090dup	NG_029043.1:g.10084_10090dup	NG_029043.1:g.10081_10090dup	NG_029043.1:g.10080_10090dup	NG_029043.1:g.10090_10091insTTTTTTTTTTTTTTTTTTTTTTTTTT	NG_029043.1:g.10090_10091insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NG_029043.1:g.10090_10091insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
APOA2 RefSeqGene	NG_012043.1:g.8243_8264=	NG_012043.1:g.8255_8264del	NG_012043.1:g.8258_8264del	NG_012043.1:g.8259_8264del	NG_012043.1:g.8260_8264del	NG_012043.1:g.8261_8264del	NG_012043.1:g.8262_8264del	NG_012043.1:g.8263_8264del	NG_012043.1:g.8264del	NG_012043.1:g.8264dup	NG_012043.1:g.8263_8264dup	NG_012043.1:g.8262_8264dup	NG_012043.1:g.8261_8264dup	NG_012043.1:g.8260_8264dup	NG_012043.1:g.8258_8264dup	NG_012043.1:g.8255_8264dup	NG_012043.1:g.8254_8264dup	NG_012043.1:g.8264_8265insAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_012043.1:g.8264_8265insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_012043.1:g.8264_8265insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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

47 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83234962	Oct 11, 2018 (152)
2	HUMANGENOME_JCVI	ss95940167	Oct 11, 2018 (152)
3	PJP	ss294606958	Oct 11, 2018 (152)
4	EVA_GENOME_DK	ss1574035643	Apr 01, 2015 (144)
5	EVA_EXAC	ss1711642723	Apr 01, 2015 (144)
6	SWEGEN	ss2987827771	Nov 08, 2017 (151)
7	SWEGEN	ss2987827772	Nov 08, 2017 (151)
8	MCHAISSO	ss3064426978	Nov 08, 2017 (151)
9	URBANLAB	ss3646801348	Oct 11, 2018 (152)
10	PACBIO	ss3794080680	Jul 12, 2019 (153)
11	EVA	ss3826448191	Apr 25, 2020 (154)
12	GNOMAD	ss4004548116	Apr 25, 2021 (155)
13	GNOMAD	ss4004548117	Apr 25, 2021 (155)
14	GNOMAD	ss4004548118	Apr 25, 2021 (155)
15	GNOMAD	ss4004548119	Apr 25, 2021 (155)
16	GNOMAD	ss4004548120	Apr 25, 2021 (155)
17	GNOMAD	ss4004548121	Apr 25, 2021 (155)
18	GNOMAD	ss4004548122	Apr 25, 2021 (155)
19	GNOMAD	ss4004548123	Apr 25, 2021 (155)
20	GNOMAD	ss4004548124	Apr 25, 2021 (155)
21	GNOMAD	ss4004548125	Apr 25, 2021 (155)
22	GNOMAD	ss4004548127	Apr 25, 2021 (155)
23	GNOMAD	ss4004548128	Apr 25, 2021 (155)
24	GNOMAD	ss4004548129	Apr 25, 2021 (155)
25	GNOMAD	ss4004548130	Apr 25, 2021 (155)
26	GNOMAD	ss4004548131	Apr 25, 2021 (155)
27	GNOMAD	ss4004548132	Apr 25, 2021 (155)
28	GNOMAD	ss4004548133	Apr 25, 2021 (155)
29	TOMMO_GENOMICS	ss5146697223	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5146697224	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5146697225	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5146697226	Apr 25, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5244453287	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5244453288	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5244453289	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5244453290	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5244453291	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5445025978	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5445025979	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5445025980	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5445025981	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5445025982	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5673959380	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5673959381	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5673959382	Oct 12, 2022 (156)
46	EVA	ss5832728729	Oct 12, 2022 (156)
47	EVA	ss5832728730	Oct 12, 2022 (156)
48	The Danish reference pan genome	NC_000001.10 - 161190155	Apr 25, 2020 (154)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 28409609 (NC_000001.11:161220364::T 26441/99870) Row 28409610 (NC_000001.11:161220364::TT 1943/99846) Row 28409611 (NC_000001.11:161220364::TTT 388/99868)...	-	Apr 25, 2021 (155)
67	gnomAD - Exomes Submission ignored due to conflicting rows: Row 1033273 (NC_000001.10:161190154::T 1/20) Row 1033274 (NC_000001.10:161190154::TT 2/20) Row 1033275 (NC_000001.10:161190154::TTT 2/20)...	-	Jul 12, 2019 (153)
68	gnomAD - Exomes Submission ignored due to conflicting rows: Row 1033273 (NC_000001.10:161190154::T 1/20) Row 1033274 (NC_000001.10:161190154::TT 2/20) Row 1033275 (NC_000001.10:161190154::TTT 2/20)...	-	Jul 12, 2019 (153)
69	gnomAD - Exomes Submission ignored due to conflicting rows: Row 1033273 (NC_000001.10:161190154::T 1/20) Row 1033274 (NC_000001.10:161190154::TT 2/20) Row 1033275 (NC_000001.10:161190154::TTT 2/20)...	-	Jul 12, 2019 (153)
70	gnomAD - Exomes Submission ignored due to conflicting rows: Row 1033273 (NC_000001.10:161190154::T 1/20) Row 1033274 (NC_000001.10:161190154::TT 2/20) Row 1033275 (NC_000001.10:161190154::TTT 2/20)...	-	Jul 12, 2019 (153)
71	gnomAD - Exomes Submission ignored due to conflicting rows: Row 1033273 (NC_000001.10:161190154::T 1/20) Row 1033274 (NC_000001.10:161190154::TT 2/20) Row 1033275 (NC_000001.10:161190154::TTT 2/20)...	-	Jul 12, 2019 (153)
72	8.3KJPN Submission ignored due to conflicting rows: Row 4666530 (NC_000001.10:161190154::T 3818/16498) Row 4666531 (NC_000001.10:161190154::TT 135/16498) Row 4666532 (NC_000001.10:161190154:T: 61/16498)...	-	Apr 25, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 4666530 (NC_000001.10:161190154::T 3818/16498) Row 4666531 (NC_000001.10:161190154::TT 135/16498) Row 4666532 (NC_000001.10:161190154:T: 61/16498)...	-	Apr 25, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 4666530 (NC_000001.10:161190154::T 3818/16498) Row 4666531 (NC_000001.10:161190154::TT 135/16498) Row 4666532 (NC_000001.10:161190154:T: 61/16498)...	-	Apr 25, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 4666530 (NC_000001.10:161190154::T 3818/16498) Row 4666531 (NC_000001.10:161190154::TT 135/16498) Row 4666532 (NC_000001.10:161190154:T: 61/16498)...	-	Apr 25, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 7796484 (NC_000001.11:161220364::T 7303/28208) Row 7796485 (NC_000001.11:161220364::TT 246/28208) Row 7796486 (NC_000001.11:161220364:T: 124/28208)	-	Oct 12, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 7796484 (NC_000001.11:161220364::T 7303/28208) Row 7796485 (NC_000001.11:161220364::TT 246/28208) Row 7796486 (NC_000001.11:161220364:T: 124/28208)	-	Oct 12, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 7796484 (NC_000001.11:161220364::T 7303/28208) Row 7796485 (NC_000001.11:161220364::TT 246/28208) Row 7796486 (NC_000001.11:161220364:T: 124/28208)	-	Oct 12, 2022 (156)
79	ALFA	NC_000001.11 - 161220365	Apr 25, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4004548133	NC_000001.11:161220364:TTTTTTTTTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5146697226	NC_000001.10:161190154:TTTTTTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4004548132, ss5445025982	NC_000001.11:161220364:TTTTTTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4004548131	NC_000001.11:161220364:TTTTTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4004548130, ss5244453291	NC_000001.11:161220364:TTTTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4004548129	NC_000001.11:161220364:TTTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4004548128	NC_000001.11:161220364:TTT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
	NC_000001.10:161190154:TT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4004548127, ss5445025981	NC_000001.11:161220364:TT:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5146697225	NC_000001.10:161190154:T:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5244453289, ss5445025980, ss5673959382	NC_000001.11:161220364:T:	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss294606958	NC_000001.9:159456800::T	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1711642723, ss2987827771, ss3826448191, ss5146697223, ss5832728730	NC_000001.10:161190154::T	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3064426978, ss4004548116, ss5244453287, ss5445025978, ss5673959380	NC_000001.11:161220364::T	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss83234962, ss95940167	NT_004487.19:12678818::T	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
175998, ss1574035643, ss2987827772, ss3794080680, ss5146697224, ss5832728729	NC_000001.10:161190154::TT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3646801348, ss4004548117, ss5244453288, ss5445025979, ss5673959381	NC_000001.11:161220364::TT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000001.10:161190154::TTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548118, ss5244453290	NC_000001.11:161220364::TTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548119	NC_000001.11:161220364::TTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548120	NC_000001.11:161220364::TTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548121	NC_000001.11:161220364::TTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548122	NC_000001.11:161220364::TTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548123	NC_000001.11:161220364::TTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548124	NC_000001.11:161220364::TTTTTTTTTT… NC_000001.11:161220364::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2768414531	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4004548125	NC_000001.11:161220364::TTTTTTTTTT… NC_000001.11:161220364::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:161220364:TTTTTTTTTTT… NC_000001.11:161220364:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs781711813

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

rs781711813