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rs765468034

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs765468034(C;T)
Make rs765468034(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18142826
GeneMYO15A
is asnp
is mentioned by
dbSNPrs765468034
ebirs765468034
HLIrs765468034
Exacrs765468034
Varsomers765468034
Maprs765468034
PheGenIrs765468034
hapmaprs765468034
1000 genomesrs765468034
hgdprs765468034
ensemblrs765468034
gopubmedrs765468034
geneviewrs765468034
scholarrs765468034
googlers765468034
pharmgkbrs765468034
gwascentralrs765468034
openSNPrs765468034
23andMers765468034
23andMe allrs765468034
SNP Nexus

SNPshotrs765468034
SNPdbers765468034
MSV3drs765468034
GWAS Ctlgrs765468034
Max Magnitude0
ClinVar
Risk rs765468034(T;T)
Alt rs765468034(T;T)
Reference rs765468034(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.18046140C>T
CLNSRC
CLNACC RCV000214976.1,