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Select item 81118021.

rs8111802 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 19:9854147 (GRCh38)
19:9964823 (GRCh37)
Canonical SPDI:: NC_000019.10:9854146:A:C,NC_000019.10:9854146:A:G,NC_000019.10:9854146:A:T
Gene:: OLFM2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.0352638/1230 (ALFA)
A=0./0 (GENOME_DK)
T=0./0 (KOREAN)
A=0.0049107/22 (Estonian)
A=0.0066667/4 (NorthernSweden)
A=0.0067422/25 (TWINSUK)
A=0.0085625/33 (ALSPAC)
A=0.0341748/47532 (GnomAD_exomes)
A=0.0555556/3 (Siberian)
A=0.0664411/864 (GoESP)
A=0.0782114/9111 (ExAC)
A=0.0796813/11880 (GnomAD_genomes)
A=0.0902376/23885 (TOPMED)
A=0.1018519/22 (Qatari)
A=0.1475096/77 (SGDP_PRJ)
A=0.1681323/13231 (PAGE_STUDY)
A=0.1777014/1138 (1000Genomes_30X)
A=0.182508/914 (1000Genomes)
A=0.2992341/547 (Korea1K)
A=0.3052559/2207 (Korea4K)
G=0.3127341/167 (MGP)
A=0.3224299/69 (Vietnamese)
A=0.3615595/27997 (TOMMO)
HGVS:: NC_000019.10:g.9854147A>C, NC_000019.10:g.9854147A>G, NC_000019.10:g.9854147A>T, NC_000019.9:g.9964823A>C, NC_000019.9:g.9964823A>G, NC_000019.9:g.9964823A>T, NM_058164.4:c.*39T>G, NM_058164.4:c.*39T>C, NM_058164.4:c.*39T>A, NM_058164.3:c.*39T>G, NM_058164.3:c.*39T>C, NM_058164.3:c.*39T>A, NM_058164.2:c.*39C>T, NM_058164.2:c.*39C>G, NM_058164.2:c.*39C>A, NM_001304347.2:c.*39T>G, NM_001304347.2:c.*39T>C, NM_001304347.2:c.*39T>A, NM_001304347.1:c.*39T>G, NM_001304347.1:c.*39T>C, NM_001304347.1:c.*39T>A, NM_001304348.2:c.*39T>G, NM_001304348.2:c.*39T>C, NM_001304348.2:c.*39T>A, NM_001304348.1:c.*39T>G, NM_001304348.1:c.*39T>C, NM_001304348.1:c.*39T>A, XM_047439713.1:c.*39T>G, XM_047439713.1:c.*39T>C, XM_047439713.1:c.*39T>A

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