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rs139956283

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139956283(A;A)
Make rs139956283(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position43600011
GeneSTRC
is asnp
is mentioned by
dbSNPrs139956283
ebirs139956283
HLIrs139956283
Exacrs139956283
Varsomers139956283
Maprs139956283
PheGenIrs139956283
hapmaprs139956283
1000 genomesrs139956283
hgdprs139956283
ensemblrs139956283
gopubmedrs139956283
geneviewrs139956283
scholarrs139956283
googlers139956283
pharmgkbrs139956283
gwascentralrs139956283
openSNPrs139956283
23andMers139956283
23andMe allrs139956283
SNP Nexus

SNPshotrs139956283
SNPdbers139956283
MSV3drs139956283
GWAS Ctlgrs139956283
Max Magnitude0
ClinVar
Risk rs139956283(A;A)
Alt rs139956283(A;A)
Reference rs139956283(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene STRC
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000015.9:g.43892209G>A
CLNSRC
CLNACC RCV000151937.1,