Name: rs71151702
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.

rs71151702

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:23203770-23203796 (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)₁₈ / del(A)₁₆ / del(A)₁₅ / d…
del(A)₁₈ / del(A)₁₆ / del(A)₁₅ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₉ / dup(A)₁₁ / dup(A)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₈=0.0000 (0/1228, ALFA)
del(A)₁₆=0.0000 (0/1228, ALFA)
del(A)₁₅=0.0000 (0/1228, ALFA) (+ 17 more)
del(A)₁₂=0.0000 (0/1228, ALFA)
del(A)₁₁=0.0000 (0/1228, ALFA)
del(A)₁₀=0.0000 (0/1228, ALFA)
del(A)₉=0.0000 (0/1228, ALFA)
del(A)₈=0.0000 (0/1228, ALFA)
del(A)₇=0.0000 (0/1228, ALFA)
del(A)₆=0.0000 (0/1228, ALFA)
del(A)₅=0.0000 (0/1228, ALFA)
del(A)₄=0.0000 (0/1228, ALFA)
delAAA=0.0000 (0/1228, ALFA)
delAA=0.0000 (0/1228, ALFA)
delA=0.0000 (0/1228, ALFA)
dupA=0.0000 (0/1228, ALFA)
dupAA=0.0000 (0/1228, ALFA)
dupAAA=0.0000 (0/1228, ALFA)
dup(A)₄=0.0000 (0/1228, ALFA)
dup(A)₅=0.0000 (0/1228, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SCNN1G : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	1228	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	594	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	538	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	514	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	22	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	54	AAAAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	1228	(A)₂₇=1.0000	del(A)₁₈=0.0000, del(A)₁₆=0.0000, del(A)₁₅=0.0000, del(A)₁₂=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)₅=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
Allele Frequency Aggregator	European	Sub	594	(A)₂₇=1.000	del(A)₁₈=0.000, del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₂=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)₅=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
Allele Frequency Aggregator	African	Sub	538	(A)₂₇=1.000	del(A)₁₈=0.000, del(A)₁₆=0.000, del(A)₁₅=0.000, del(A)₁₂=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)₅=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
Allele Frequency Aggregator	Other	Sub	54	(A)₂₇=1.00	del(A)₁₈=0.00, del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₂=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)₅=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
Allele Frequency Aggregator	Latin American 1	Sub	22	(A)₂₇=1.00	del(A)₁₈=0.00, del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₂=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)₅=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
Allele Frequency Aggregator	Latin American 2	Sub	14	(A)₂₇=1.00	del(A)₁₈=0.00, del(A)₁₆=0.00, del(A)₁₅=0.00, del(A)₁₂=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)₅=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
Allele Frequency Aggregator	South Asian	Sub	4	(A)₂₇=1.0	del(A)₁₈=0.0, del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Asian	Sub	2	(A)₂₇=1.0	del(A)₁₈=0.0, del(A)₁₆=0.0, del(A)₁₅=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0

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 16	NC_000016.10:g.23203779_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203781_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203782_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203785_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203786_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203787_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203788_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203789_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203790_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203791_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203792_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203793_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203794_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203795_23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203796del
GRCh38.p14 chr 16	NC_000016.10:g.23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203795_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203794_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203793_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203792_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203791_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203788_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203786_23203796dup
GRCh38.p14 chr 16	NC_000016.10:g.23203784_23203796dup
GRCh37.p13 chr 16	NC_000016.9:g.23215100_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215102_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215103_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215106_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215107_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215108_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215109_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215110_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215111_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215112_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215113_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215114_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215115_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215116_23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215117del
GRCh37.p13 chr 16	NC_000016.9:g.23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215116_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215115_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215114_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215113_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215112_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215109_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215107_23215117dup
GRCh37.p13 chr 16	NC_000016.9:g.23215105_23215117dup
SCNN1G RefSeqGene	NG_011909.1:g.26061_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26063_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26064_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26067_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26068_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26069_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26070_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26071_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26072_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26073_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26074_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26075_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26076_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26077_26078del
SCNN1G RefSeqGene	NG_011909.1:g.26078del
SCNN1G RefSeqGene	NG_011909.1:g.26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26077_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26076_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26075_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26074_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26073_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26070_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26068_26078dup
SCNN1G RefSeqGene	NG_011909.1:g.26066_26078dup

Gene: SCNN1G, sodium channel epithelial 1 subunit gamma (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SCNN1G transcript	NM_001039.4:c.1078-5971_1… NM_001039.4:c.1078-5971_1078-5954del	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)₂₇=	del(A)₁₈	del(A)₁₆	del(A)₁₅	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₉	dup(A)₁₁	dup(A)₁₃
GRCh38.p14 chr 16	NC_000016.10:g.23203770_23203796=	NC_000016.10:g.23203779_23203796del	NC_000016.10:g.23203781_23203796del	NC_000016.10:g.23203782_23203796del	NC_000016.10:g.23203785_23203796del	NC_000016.10:g.23203786_23203796del	NC_000016.10:g.23203787_23203796del	NC_000016.10:g.23203788_23203796del	NC_000016.10:g.23203789_23203796del	NC_000016.10:g.23203790_23203796del	NC_000016.10:g.23203791_23203796del	NC_000016.10:g.23203792_23203796del	NC_000016.10:g.23203793_23203796del	NC_000016.10:g.23203794_23203796del	NC_000016.10:g.23203795_23203796del	NC_000016.10:g.23203796del	NC_000016.10:g.23203796dup	NC_000016.10:g.23203795_23203796dup	NC_000016.10:g.23203794_23203796dup	NC_000016.10:g.23203793_23203796dup	NC_000016.10:g.23203792_23203796dup	NC_000016.10:g.23203791_23203796dup	NC_000016.10:g.23203788_23203796dup	NC_000016.10:g.23203786_23203796dup	NC_000016.10:g.23203784_23203796dup
GRCh37.p13 chr 16	NC_000016.9:g.23215091_23215117=	NC_000016.9:g.23215100_23215117del	NC_000016.9:g.23215102_23215117del	NC_000016.9:g.23215103_23215117del	NC_000016.9:g.23215106_23215117del	NC_000016.9:g.23215107_23215117del	NC_000016.9:g.23215108_23215117del	NC_000016.9:g.23215109_23215117del	NC_000016.9:g.23215110_23215117del	NC_000016.9:g.23215111_23215117del	NC_000016.9:g.23215112_23215117del	NC_000016.9:g.23215113_23215117del	NC_000016.9:g.23215114_23215117del	NC_000016.9:g.23215115_23215117del	NC_000016.9:g.23215116_23215117del	NC_000016.9:g.23215117del	NC_000016.9:g.23215117dup	NC_000016.9:g.23215116_23215117dup	NC_000016.9:g.23215115_23215117dup	NC_000016.9:g.23215114_23215117dup	NC_000016.9:g.23215113_23215117dup	NC_000016.9:g.23215112_23215117dup	NC_000016.9:g.23215109_23215117dup	NC_000016.9:g.23215107_23215117dup	NC_000016.9:g.23215105_23215117dup
SCNN1G RefSeqGene	NG_011909.1:g.26052_26078=	NG_011909.1:g.26061_26078del	NG_011909.1:g.26063_26078del	NG_011909.1:g.26064_26078del	NG_011909.1:g.26067_26078del	NG_011909.1:g.26068_26078del	NG_011909.1:g.26069_26078del	NG_011909.1:g.26070_26078del	NG_011909.1:g.26071_26078del	NG_011909.1:g.26072_26078del	NG_011909.1:g.26073_26078del	NG_011909.1:g.26074_26078del	NG_011909.1:g.26075_26078del	NG_011909.1:g.26076_26078del	NG_011909.1:g.26077_26078del	NG_011909.1:g.26078del	NG_011909.1:g.26078dup	NG_011909.1:g.26077_26078dup	NG_011909.1:g.26076_26078dup	NG_011909.1:g.26075_26078dup	NG_011909.1:g.26074_26078dup	NG_011909.1:g.26073_26078dup	NG_011909.1:g.26070_26078dup	NG_011909.1:g.26068_26078dup	NG_011909.1:g.26066_26078dup
SCNN1G transcript	NM_001039.3:c.1078-5980=	NM_001039.3:c.1078-5971_1078-5954del	NM_001039.3:c.1078-5969_1078-5954del	NM_001039.3:c.1078-5968_1078-5954del	NM_001039.3:c.1078-5965_1078-5954del	NM_001039.3:c.1078-5964_1078-5954del	NM_001039.3:c.1078-5963_1078-5954del	NM_001039.3:c.1078-5962_1078-5954del	NM_001039.3:c.1078-5961_1078-5954del	NM_001039.3:c.1078-5960_1078-5954del	NM_001039.3:c.1078-5959_1078-5954del	NM_001039.3:c.1078-5958_1078-5954del	NM_001039.3:c.1078-5957_1078-5954del	NM_001039.3:c.1078-5956_1078-5954del	NM_001039.3:c.1078-5955_1078-5954del	NM_001039.3:c.1078-5954del	NM_001039.3:c.1078-5954dup	NM_001039.3:c.1078-5955_1078-5954dup	NM_001039.3:c.1078-5956_1078-5954dup	NM_001039.3:c.1078-5957_1078-5954dup	NM_001039.3:c.1078-5958_1078-5954dup	NM_001039.3:c.1078-5959_1078-5954dup	NM_001039.3:c.1078-5962_1078-5954dup	NM_001039.3:c.1078-5964_1078-5954dup	NM_001039.3:c.1078-5966_1078-5954dup
SCNN1G transcript	NM_001039.4:c.1078-5980=	NM_001039.4:c.1078-5971_1078-5954del	NM_001039.4:c.1078-5969_1078-5954del	NM_001039.4:c.1078-5968_1078-5954del	NM_001039.4:c.1078-5965_1078-5954del	NM_001039.4:c.1078-5964_1078-5954del	NM_001039.4:c.1078-5963_1078-5954del	NM_001039.4:c.1078-5962_1078-5954del	NM_001039.4:c.1078-5961_1078-5954del	NM_001039.4:c.1078-5960_1078-5954del	NM_001039.4:c.1078-5959_1078-5954del	NM_001039.4:c.1078-5958_1078-5954del	NM_001039.4:c.1078-5957_1078-5954del	NM_001039.4:c.1078-5956_1078-5954del	NM_001039.4:c.1078-5955_1078-5954del	NM_001039.4:c.1078-5954del	NM_001039.4:c.1078-5954dup	NM_001039.4:c.1078-5955_1078-5954dup	NM_001039.4:c.1078-5956_1078-5954dup	NM_001039.4:c.1078-5957_1078-5954dup	NM_001039.4:c.1078-5958_1078-5954dup	NM_001039.4:c.1078-5959_1078-5954dup	NM_001039.4:c.1078-5962_1078-5954dup	NM_001039.4:c.1078-5964_1078-5954dup	NM_001039.4:c.1078-5966_1078-5954dup
SCNN1G transcript variant X1	XM_005255468.1:c.1078-5980=	XM_005255468.1:c.1078-5971_1078-5954del	XM_005255468.1:c.1078-5969_1078-5954del	XM_005255468.1:c.1078-5968_1078-5954del	XM_005255468.1:c.1078-5965_1078-5954del	XM_005255468.1:c.1078-5964_1078-5954del	XM_005255468.1:c.1078-5963_1078-5954del	XM_005255468.1:c.1078-5962_1078-5954del	XM_005255468.1:c.1078-5961_1078-5954del	XM_005255468.1:c.1078-5960_1078-5954del	XM_005255468.1:c.1078-5959_1078-5954del	XM_005255468.1:c.1078-5958_1078-5954del	XM_005255468.1:c.1078-5957_1078-5954del	XM_005255468.1:c.1078-5956_1078-5954del	XM_005255468.1:c.1078-5955_1078-5954del	XM_005255468.1:c.1078-5954del	XM_005255468.1:c.1078-5954dup	XM_005255468.1:c.1078-5955_1078-5954dup	XM_005255468.1:c.1078-5956_1078-5954dup	XM_005255468.1:c.1078-5957_1078-5954dup	XM_005255468.1:c.1078-5958_1078-5954dup	XM_005255468.1:c.1078-5959_1078-5954dup	XM_005255468.1:c.1078-5962_1078-5954dup	XM_005255468.1:c.1078-5964_1078-5954dup	XM_005255468.1:c.1078-5966_1078-5954dup
SCNN1G transcript variant X2	XM_005255469.1:c.1077+6343=	XM_005255469.1:c.1077+6352_1077+6369del	XM_005255469.1:c.1077+6354_1077+6369del	XM_005255469.1:c.1077+6355_1077+6369del	XM_005255469.1:c.1077+6358_1077+6369del	XM_005255469.1:c.1077+6359_1077+6369del	XM_005255469.1:c.1077+6360_1077+6369del	XM_005255469.1:c.1077+6361_1077+6369del	XM_005255469.1:c.1077+6362_1077+6369del	XM_005255469.1:c.1077+6363_1077+6369del	XM_005255469.1:c.1077+6364_1077+6369del	XM_005255469.1:c.1077+6365_1077+6369del	XM_005255469.1:c.1077+6366_1077+6369del	XM_005255469.1:c.1077+6367_1077+6369del	XM_005255469.1:c.1077+6368_1077+6369del	XM_005255469.1:c.1077+6369del	XM_005255469.1:c.1077+6369dup	XM_005255469.1:c.1077+6368_1077+6369dup	XM_005255469.1:c.1077+6367_1077+6369dup	XM_005255469.1:c.1077+6366_1077+6369dup	XM_005255469.1:c.1077+6365_1077+6369dup	XM_005255469.1:c.1077+6364_1077+6369dup	XM_005255469.1:c.1077+6361_1077+6369dup	XM_005255469.1:c.1077+6359_1077+6369dup	XM_005255469.1:c.1077+6357_1077+6369dup

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, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95674570	Feb 13, 2009 (130)
2	PJP	ss294884271	May 09, 2011 (137)
3	PJP	ss294884272	May 09, 2011 (135)
4	SSMP	ss664306888	Apr 01, 2015 (144)
5	SWEGEN	ss3014241620	Nov 17, 2017 (151)
6	URBANLAB	ss3650486894	Oct 12, 2018 (152)
7	PACBIO	ss3792996825	Jul 13, 2019 (153)
8	PACBIO	ss3797881729	Jul 13, 2019 (153)
9	EVA	ss3834520931	Apr 27, 2020 (154)
10	GNOMAD	ss4298571903	Apr 26, 2021 (155)
11	GNOMAD	ss4298571904	Apr 26, 2021 (155)
12	GNOMAD	ss4298571905	Apr 26, 2021 (155)
13	GNOMAD	ss4298571906	Apr 26, 2021 (155)
14	GNOMAD	ss4298571907	Apr 26, 2021 (155)
15	GNOMAD	ss4298571908	Apr 26, 2021 (155)
16	GNOMAD	ss4298571909	Apr 26, 2021 (155)
17	GNOMAD	ss4298571910	Apr 26, 2021 (155)
18	GNOMAD	ss4298571911	Apr 26, 2021 (155)
19	GNOMAD	ss4298571912	Apr 26, 2021 (155)
20	GNOMAD	ss4298571913	Apr 26, 2021 (155)
21	GNOMAD	ss4298571914	Apr 26, 2021 (155)
22	GNOMAD	ss4298571915	Apr 26, 2021 (155)
23	GNOMAD	ss4298571916	Apr 26, 2021 (155)
24	GNOMAD	ss4298571917	Apr 26, 2021 (155)
25	GNOMAD	ss4298571918	Apr 26, 2021 (155)
26	GNOMAD	ss4298571919	Apr 26, 2021 (155)
27	GNOMAD	ss4298571920	Apr 26, 2021 (155)
28	GNOMAD	ss4298571921	Apr 26, 2021 (155)
29	GNOMAD	ss4298571922	Apr 26, 2021 (155)
30	GNOMAD	ss4298571923	Apr 26, 2021 (155)
31	GNOMAD	ss4298571924	Apr 26, 2021 (155)
32	GNOMAD	ss4298571925	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5218918064	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5218918065	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5218918066	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5218918067	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5218918068	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5218918069	Apr 26, 2021 (155)
39	HUGCELL_USP	ss5493947061	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5493947062	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5493947063	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5493947064	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5773541352	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5773541354	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5773541355	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5773541356	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5773541357	Oct 16, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485709721 (NC_000016.10:23203769::A 30964/39994) Row 485709722 (NC_000016.10:23203769::AA 2061/39978) Row 485709723 (NC_000016.10:23203769::AAA 209/40012)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 76887371 (NC_000016.9:23215090::A 4166/11874) Row 76887372 (NC_000016.9:23215090:AAAAAAAAAAA: 5/11874) Row 76887373 (NC_000016.9:23215090::AA 451/11874)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 76887371 (NC_000016.9:23215090::A 4166/11874) Row 76887372 (NC_000016.9:23215090:AAAAAAAAAAA: 5/11874) Row 76887373 (NC_000016.9:23215090::AA 451/11874)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 76887371 (NC_000016.9:23215090::A 4166/11874) Row 76887372 (NC_000016.9:23215090:AAAAAAAAAAA: 5/11874) Row 76887373 (NC_000016.9:23215090::AA 451/11874)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 76887371 (NC_000016.9:23215090::A 4166/11874) Row 76887372 (NC_000016.9:23215090:AAAAAAAAAAA: 5/11874) Row 76887373 (NC_000016.9:23215090::AA 451/11874)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 76887371 (NC_000016.9:23215090::A 4166/11874) Row 76887372 (NC_000016.9:23215090:AAAAAAAAAAA: 5/11874) Row 76887373 (NC_000016.9:23215090::AA 451/11874)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 76887371 (NC_000016.9:23215090::A 4166/11874) Row 76887372 (NC_000016.9:23215090:AAAAAAAAAAA: 5/11874) Row 76887373 (NC_000016.9:23215090::AA 451/11874)...	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 107378456 (NC_000016.10:23203769::A 8454/21168) Row 107378458 (NC_000016.10:23203769::AA 911/21168) Row 107378459 (NC_000016.10:23203769:AA: 436/21168)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 107378456 (NC_000016.10:23203769::A 8454/21168) Row 107378458 (NC_000016.10:23203769::AA 911/21168) Row 107378459 (NC_000016.10:23203769:AA: 436/21168)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 107378456 (NC_000016.10:23203769::A 8454/21168) Row 107378458 (NC_000016.10:23203769::AA 911/21168) Row 107378459 (NC_000016.10:23203769:AA: 436/21168)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 107378456 (NC_000016.10:23203769::A 8454/21168) Row 107378458 (NC_000016.10:23203769::AA 911/21168) Row 107378459 (NC_000016.10:23203769:AA: 436/21168)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 107378456 (NC_000016.10:23203769::A 8454/21168) Row 107378458 (NC_000016.10:23203769::AA 911/21168) Row 107378459 (NC_000016.10:23203769:AA: 436/21168)...	-	Oct 16, 2022 (156)
82	ALFA	NC_000016.10 - 23203770	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)
rs138220316	Sep 17, 2011 (135)
rs150368217	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4298571925	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4298571924	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4298571923	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4298571922	NC_000016.10:23203769:AAAAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5218918065	NC_000016.9:23215090:AAAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4298571921	NC_000016.10:23203769:AAAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4298571920	NC_000016.10:23203769:AAAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4298571919	NC_000016.10:23203769:AAAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4298571918	NC_000016.10:23203769:AAAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4298571917	NC_000016.10:23203769:AAAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4298571916	NC_000016.10:23203769:AAAAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571915	NC_000016.10:23203769:AAAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571914	NC_000016.10:23203769:AAA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3014241620, ss5218918067	NC_000016.9:23215090:AA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571913, ss5493947064, ss5773541355	NC_000016.10:23203769:AA:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5218918069	NC_000016.9:23215090:A:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571912, ss5493947062, ss5773541357	NC_000016.10:23203769:A:	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294884271	NC_000016.8:23122592::A	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294884272	NC_000016.8:23122618::A	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss664306888, ss3792996825, ss3797881729, ss5218918064	NC_000016.9:23215090::A	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571903, ss5493947061, ss5773541352	NC_000016.10:23203769::A	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95674570	NT_010393.16:23155117::A	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3834520931, ss5218918066	NC_000016.9:23215090::AA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571904, ss5493947063, ss5773541354	NC_000016.10:23203769::AA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5218918068	NC_000016.9:23215090::AAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571905, ss5773541356	NC_000016.10:23203769::AAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3650486894	NC_000016.10:23203790::AAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571906	NC_000016.10:23203769::AAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571907	NC_000016.10:23203769::AAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2328361636	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571908	NC_000016.10:23203769::AAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571909	NC_000016.10:23203769::AAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571910	NC_000016.10:23203769::AAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4298571911	NC_000016.10:23203769::AAAAAAAAAAA… NC_000016.10:23203769::AAAAAAAAAAAAA	NC_000016.10:23203769:AAAAAAAAAAAA… NC_000016.10:23203769:AAAAAAAAAAAAAAAAAAAAAAAAAAA: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 rs71151702

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

rs71151702