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rs373462792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373462792(C;T)
Make rs373462792(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18157209
GeneMYO15A
is asnp
is mentioned by
dbSNPrs373462792
ebirs373462792
HLIrs373462792
Exacrs373462792
Varsomers373462792
Maprs373462792
PheGenIrs373462792
hapmaprs373462792
1000 genomesrs373462792
hgdprs373462792
ensemblrs373462792
gopubmedrs373462792
geneviewrs373462792
scholarrs373462792
googlers373462792
pharmgkbrs373462792
gwascentralrs373462792
openSNPrs373462792
23andMers373462792
23andMe allrs373462792
SNP Nexus

SNPshotrs373462792
SNPdbers373462792
MSV3drs373462792
GWAS Ctlgrs373462792
Max Magnitude0
ClinVar
Risk rs373462792(T;T)
Alt rs373462792(T;T)
Reference rs373462792(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18060523C>T
CLNSRC ClinVar
CLNACC RCV000038995.3,