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rs377015931

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377015931(A;A)
Make rs377015931(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position18157155
GeneMYO15A
is asnp
is mentioned by
dbSNPrs377015931
ebirs377015931
HLIrs377015931
Exacrs377015931
Varsomers377015931
Maprs377015931
PheGenIrs377015931
hapmaprs377015931
1000 genomesrs377015931
hgdprs377015931
ensemblrs377015931
gopubmedrs377015931
geneviewrs377015931
scholarrs377015931
googlers377015931
pharmgkbrs377015931
gwascentralrs377015931
openSNPrs377015931
23andMers377015931
23andMe allrs377015931
SNP Nexus

SNPshotrs377015931
SNPdbers377015931
MSV3drs377015931
GWAS Ctlgrs377015931
Max Magnitude0
ClinVar
Risk rs377015931(A;A)
Alt rs377015931(A;A)
Reference rs377015931(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18060469G>A
CLNSRC
CLNACC RCV000155197.1,