Name: rs60491859
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.

rs60491859

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:51862710-51862729 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₃ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₃ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₂ / dup(A)₁₃ / dup(A)₁₄ / dup(A)₁₅ / dup(A)₁₆ / dup(A)₁₇ / dup(A)₁₈ / dup(A)₁₉ / dup(A)₂₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₀=0.000019 (5/264690, TOPMED)
del(A)₁₃=0.0000 (0/7528, ALFA)
del(A)₁₁=0.0000 (0/7528, ALFA) (+ 15 more)
del(A)₁₀=0.0000 (0/7528, ALFA)
del(A)₉=0.0000 (0/7528, ALFA)
del(A)₈=0.0000 (0/7528, ALFA)
del(A)₇=0.0000 (0/7528, ALFA)
del(A)₆=0.0000 (0/7528, ALFA)
del(A)₄=0.0000 (0/7528, ALFA)
delAAA=0.0000 (0/7528, ALFA)
delAA=0.0000 (0/7528, ALFA)
delA=0.0000 (0/7528, ALFA)
dupA=0.0000 (0/7528, ALFA)
dupAA=0.0000 (0/7528, ALFA)
dupAAA=0.0000 (0/7528, ALFA)
dup(A)₄=0.0000 (0/7528, ALFA)
dup(A)₅=0.0000 (0/7528, ALFA)
dup(A)₆=0.0000 (0/7528, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01429 : 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	HWEP
Total	Global	7528	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	5766	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1028	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	36	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	992	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	88	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	70	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	18	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	54	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	280	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	62	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	250	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₀=0.999981	del(A)₁₀=0.000019
Allele Frequency Aggregator	Total	Global	7528	(A)₂₀=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	5766	(A)₂₀=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	1028	(A)₂₀=1.0000	del(A)₁₃=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	280	(A)₂₀=1.000	del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Other	Sub	250	(A)₂₀=1.000	del(A)₁₃=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Asian	Sub	88	(A)₂₀=1.00	del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(A)₂₀=1.00	del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	54	(A)₂₀=1.00	del(A)₁₃=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00

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 20	NC_000020.11:g.51862717_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862719_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862720_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862721_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862722_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862723_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862724_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862726_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862727_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862728_51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862729del
GRCh38.p14 chr 20	NC_000020.11:g.51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862728_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862727_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862726_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862725_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862724_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862723_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862722_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862720_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862719_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862718_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862717_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862716_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862715_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862714_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862713_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862712_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862711_51862729dup
GRCh38.p14 chr 20	NC_000020.11:g.51862710_51862729dup
GRCh37.p13 chr 20	NC_000020.10:g.50479256_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479258_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479259_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479260_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479261_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479262_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479263_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479265_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479266_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479267_50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479268del
GRCh37.p13 chr 20	NC_000020.10:g.50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479267_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479266_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479265_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479264_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479263_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479262_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479261_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479259_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479258_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479257_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479256_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479255_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479254_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479253_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479252_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479251_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479250_50479268dup
GRCh37.p13 chr 20	NC_000020.10:g.50479249_50479268dup

Gene: LINC01429, long intergenic non-protein coding RNA 1429 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01429 transcript	NR_110016.1:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(A)₂₀=	del(A)₁₃	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₁₀	dup(A)₁₁	dup(A)₁₂	dup(A)₁₃	dup(A)₁₄	dup(A)₁₅	dup(A)₁₆	dup(A)₁₇	dup(A)₁₈	dup(A)₁₉	dup(A)₂₀
GRCh38.p14 chr 20	NC_000020.11:g.51862710_51862729=	NC_000020.11:g.51862717_51862729del	NC_000020.11:g.51862719_51862729del	NC_000020.11:g.51862720_51862729del	NC_000020.11:g.51862721_51862729del	NC_000020.11:g.51862722_51862729del	NC_000020.11:g.51862723_51862729del	NC_000020.11:g.51862724_51862729del	NC_000020.11:g.51862726_51862729del	NC_000020.11:g.51862727_51862729del	NC_000020.11:g.51862728_51862729del	NC_000020.11:g.51862729del	NC_000020.11:g.51862729dup	NC_000020.11:g.51862728_51862729dup	NC_000020.11:g.51862727_51862729dup	NC_000020.11:g.51862726_51862729dup	NC_000020.11:g.51862725_51862729dup	NC_000020.11:g.51862724_51862729dup	NC_000020.11:g.51862723_51862729dup	NC_000020.11:g.51862722_51862729dup	NC_000020.11:g.51862720_51862729dup	NC_000020.11:g.51862719_51862729dup	NC_000020.11:g.51862718_51862729dup	NC_000020.11:g.51862717_51862729dup	NC_000020.11:g.51862716_51862729dup	NC_000020.11:g.51862715_51862729dup	NC_000020.11:g.51862714_51862729dup	NC_000020.11:g.51862713_51862729dup	NC_000020.11:g.51862712_51862729dup	NC_000020.11:g.51862711_51862729dup	NC_000020.11:g.51862710_51862729dup
GRCh37.p13 chr 20	NC_000020.10:g.50479249_50479268=	NC_000020.10:g.50479256_50479268del	NC_000020.10:g.50479258_50479268del	NC_000020.10:g.50479259_50479268del	NC_000020.10:g.50479260_50479268del	NC_000020.10:g.50479261_50479268del	NC_000020.10:g.50479262_50479268del	NC_000020.10:g.50479263_50479268del	NC_000020.10:g.50479265_50479268del	NC_000020.10:g.50479266_50479268del	NC_000020.10:g.50479267_50479268del	NC_000020.10:g.50479268del	NC_000020.10:g.50479268dup	NC_000020.10:g.50479267_50479268dup	NC_000020.10:g.50479266_50479268dup	NC_000020.10:g.50479265_50479268dup	NC_000020.10:g.50479264_50479268dup	NC_000020.10:g.50479263_50479268dup	NC_000020.10:g.50479262_50479268dup	NC_000020.10:g.50479261_50479268dup	NC_000020.10:g.50479259_50479268dup	NC_000020.10:g.50479258_50479268dup	NC_000020.10:g.50479257_50479268dup	NC_000020.10:g.50479256_50479268dup	NC_000020.10:g.50479255_50479268dup	NC_000020.10:g.50479254_50479268dup	NC_000020.10:g.50479253_50479268dup	NC_000020.10:g.50479252_50479268dup	NC_000020.10:g.50479251_50479268dup	NC_000020.10:g.50479250_50479268dup	NC_000020.10:g.50479249_50479268dup

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#.

69 SubSNP, 43 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80494812	Dec 15, 2007 (129)
2	HGSV	ss80977719	Dec 15, 2007 (129)
3	HGSV	ss82211774	Dec 15, 2007 (129)
4	HGSV	ss83003921	Dec 15, 2007 (129)
5	SSMP	ss664481744	Apr 01, 2015 (144)
6	SSIP	ss947405651	Aug 21, 2014 (142)
7	SWEGEN	ss3018324705	Nov 08, 2017 (151)
8	SWEGEN	ss3018324706	Nov 08, 2017 (151)
9	SWEGEN	ss3018324707	Nov 08, 2017 (151)
10	SWEGEN	ss3018324708	Nov 08, 2017 (151)
11	EVA_DECODE	ss3707122738	Jul 13, 2019 (153)
12	EVA_DECODE	ss3707122739	Jul 13, 2019 (153)
13	EVA_DECODE	ss3707122740	Jul 13, 2019 (153)
14	EVA_DECODE	ss3707122741	Jul 13, 2019 (153)
15	PACBIO	ss3788670847	Jul 13, 2019 (153)
16	PACBIO	ss3798445174	Jul 13, 2019 (153)
17	EVA	ss3835715699	Apr 27, 2020 (154)
18	GNOMAD	ss4354913319	Apr 27, 2021 (155)
19	GNOMAD	ss4354913320	Apr 27, 2021 (155)
20	GNOMAD	ss4354913321	Apr 27, 2021 (155)
21	GNOMAD	ss4354913322	Apr 27, 2021 (155)
22	GNOMAD	ss4354913323	Apr 27, 2021 (155)
23	GNOMAD	ss4354913324	Apr 27, 2021 (155)
24	GNOMAD	ss4354913325	Apr 27, 2021 (155)
25	GNOMAD	ss4354913326	Apr 27, 2021 (155)
26	GNOMAD	ss4354913327	Apr 27, 2021 (155)
27	GNOMAD	ss4354913328	Apr 27, 2021 (155)
28	GNOMAD	ss4354913329	Apr 27, 2021 (155)
29	GNOMAD	ss4354913330	Apr 27, 2021 (155)
30	GNOMAD	ss4354913331	Apr 27, 2021 (155)
31	GNOMAD	ss4354913332	Apr 27, 2021 (155)
32	GNOMAD	ss4354913333	Apr 27, 2021 (155)
33	GNOMAD	ss4354913334	Apr 27, 2021 (155)
34	GNOMAD	ss4354913335	Apr 27, 2021 (155)
35	GNOMAD	ss4354913336	Apr 27, 2021 (155)
36	GNOMAD	ss4354913337	Apr 27, 2021 (155)
37	GNOMAD	ss4354913339	Apr 27, 2021 (155)
38	GNOMAD	ss4354913340	Apr 27, 2021 (155)
39	GNOMAD	ss4354913341	Apr 27, 2021 (155)
40	GNOMAD	ss4354913342	Apr 27, 2021 (155)
41	GNOMAD	ss4354913343	Apr 27, 2021 (155)
42	GNOMAD	ss4354913344	Apr 27, 2021 (155)
43	GNOMAD	ss4354913345	Apr 27, 2021 (155)
44	GNOMAD	ss4354913346	Apr 27, 2021 (155)
45	GNOMAD	ss4354913347	Apr 27, 2021 (155)
46	GNOMAD	ss4354913348	Apr 27, 2021 (155)
47	GNOMAD	ss4354913349	Apr 27, 2021 (155)
48	TOPMED	ss5091637215	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5230055016	Apr 27, 2021 (155)
50	TOMMO_GENOMICS	ss5230055017	Apr 27, 2021 (155)
51	TOMMO_GENOMICS	ss5230055018	Apr 27, 2021 (155)
52	TOMMO_GENOMICS	ss5230055019	Apr 27, 2021 (155)
53	TOMMO_GENOMICS	ss5230055020	Apr 27, 2021 (155)
54	TOMMO_GENOMICS	ss5230055021	Apr 27, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5309110323	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5309110324	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5309110326	Oct 13, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5309110327	Oct 13, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5309110328	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5501358752	Oct 13, 2022 (156)
61	HUGCELL_USP	ss5501358753	Oct 13, 2022 (156)
62	HUGCELL_USP	ss5501358754	Oct 13, 2022 (156)
63	HUGCELL_USP	ss5501358755	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5789984124	Oct 13, 2022 (156)
65	TOMMO_GENOMICS	ss5789984125	Oct 13, 2022 (156)
66	TOMMO_GENOMICS	ss5789984126	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5789984127	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5789984128	Oct 13, 2022 (156)
69	EVA	ss5981093599	Oct 13, 2022 (156)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 554390081 (NC_000020.11:51862709::A 501/64004) Row 554390082 (NC_000020.11:51862709::AA 28/64146) Row 554390083 (NC_000020.11:51862709::AAA 11646/63928)...	-	Apr 27, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 88024323 (NC_000020.10:50479248::AAAA 399/16406) Row 88024324 (NC_000020.10:50479248::AAA 1295/16406) Row 88024325 (NC_000020.10:50479248::A 86/16406)...	-	Apr 27, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 88024323 (NC_000020.10:50479248::AAAA 399/16406) Row 88024324 (NC_000020.10:50479248::AAA 1295/16406) Row 88024325 (NC_000020.10:50479248::A 86/16406)...	-	Apr 27, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 88024323 (NC_000020.10:50479248::AAAA 399/16406) Row 88024324 (NC_000020.10:50479248::AAA 1295/16406) Row 88024325 (NC_000020.10:50479248::A 86/16406)...	-	Apr 27, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 88024323 (NC_000020.10:50479248::AAAA 399/16406) Row 88024324 (NC_000020.10:50479248::AAA 1295/16406) Row 88024325 (NC_000020.10:50479248::A 86/16406)...	-	Apr 27, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 88024323 (NC_000020.10:50479248::AAAA 399/16406) Row 88024324 (NC_000020.10:50479248::AAA 1295/16406) Row 88024325 (NC_000020.10:50479248::A 86/16406)...	-	Apr 27, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 88024323 (NC_000020.10:50479248::AAAA 399/16406) Row 88024324 (NC_000020.10:50479248::AAA 1295/16406) Row 88024325 (NC_000020.10:50479248::A 86/16406)...	-	Apr 27, 2021 (155)
106	14KJPN Submission ignored due to conflicting rows: Row 123821228 (NC_000020.11:51862709::A 141/27532) Row 123821229 (NC_000020.11:51862709::AAA 2097/27532) Row 123821230 (NC_000020.11:51862709::AAAA 589/27532)...	-	Oct 13, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 123821228 (NC_000020.11:51862709::A 141/27532) Row 123821229 (NC_000020.11:51862709::AAA 2097/27532) Row 123821230 (NC_000020.11:51862709::AAAA 589/27532)...	-	Oct 13, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 123821228 (NC_000020.11:51862709::A 141/27532) Row 123821229 (NC_000020.11:51862709::AAA 2097/27532) Row 123821230 (NC_000020.11:51862709::AAAA 589/27532)...	-	Oct 13, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 123821228 (NC_000020.11:51862709::A 141/27532) Row 123821229 (NC_000020.11:51862709::AAA 2097/27532) Row 123821230 (NC_000020.11:51862709::AAAA 589/27532)...	-	Oct 13, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 123821228 (NC_000020.11:51862709::A 141/27532) Row 123821229 (NC_000020.11:51862709::AAA 2097/27532) Row 123821230 (NC_000020.11:51862709::AAAA 589/27532)...	-	Oct 13, 2022 (156)
111	TopMed	NC_000020.11 - 51862710	Apr 27, 2021 (155)
112	ALFA	NC_000020.11 - 51862710	Apr 27, 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
ss4354913349	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
ss4354913348	NC_000020.11:51862709:AAAAAAAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
366746160, ss4354913347, ss5091637215	NC_000020.11:51862709:AAAAAAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4354913346	NC_000020.11:51862709:AAAAAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4354913345	NC_000020.11:51862709:AAAAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4354913344	NC_000020.11:51862709:AAAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4354913343	NC_000020.11:51862709:AAAAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4354913342	NC_000020.11:51862709:AAAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4354913341	NC_000020.11:51862709:AAA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4354913340	NC_000020.11:51862709:AA:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5230055021	NC_000020.10:50479248:A:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4354913339, ss5309110328, ss5789984127	NC_000020.11:51862709:A:	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss947405651, ss5230055018	NC_000020.10:50479248::A	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3707122741, ss4354913319, ss5309110326, ss5501358755, ss5789984124	NC_000020.11:51862709::A	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913320	NC_000020.11:51862709::AA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss664481744, ss3018324708, ss3788670847, ss3798445174, ss5230055017	NC_000020.10:50479248::AAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707122740, ss4354913321, ss5309110324, ss5501358752, ss5789984125	NC_000020.11:51862709::AAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80977719, ss82211774, ss83003921	NT_011362.10:20675360::AAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3018324705, ss3835715699, ss5230055016, ss5981093599	NC_000020.10:50479248::AAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707122739, ss4354913322, ss5309110323, ss5501358753, ss5789984126	NC_000020.11:51862709::AAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80494812	NT_011362.10:20675360::AAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3018324706, ss5230055019	NC_000020.10:50479248::AAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707122738, ss4354913323, ss5309110327, ss5501358754, ss5789984128	NC_000020.11:51862709::AAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3018324707	NC_000020.10:50479248::AAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913324	NC_000020.11:51862709::AAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
528322987	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913325	NC_000020.11:51862709::AAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5230055020	NC_000020.10:50479248::AAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913326	NC_000020.11:51862709::AAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913327	NC_000020.11:51862709::AAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913328	NC_000020.11:51862709::AAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913329	NC_000020.11:51862709::AAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913330	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913331	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913332	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913333	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913334	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913335	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913336	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4354913337	NC_000020.11:51862709::AAAAAAAAAAA… NC_000020.11:51862709::AAAAAAAAAAAAAAAAAAAA	NC_000020.11:51862709:AAAAAAAAAAAA… NC_000020.11:51862709:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs60491859

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

rs60491859