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rs749465098

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749465098(C;T)
Make rs749465098(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18142238
GeneMYO15A
is asnp
is mentioned by
dbSNPrs749465098
ebirs749465098
HLIrs749465098
Exacrs749465098
Varsomers749465098
Maprs749465098
PheGenIrs749465098
hapmaprs749465098
1000 genomesrs749465098
hgdprs749465098
ensemblrs749465098
gopubmedrs749465098
geneviewrs749465098
scholarrs749465098
googlers749465098
pharmgkbrs749465098
gwascentralrs749465098
openSNPrs749465098
23andMers749465098
23andMe allrs749465098
SNP Nexus

SNPshotrs749465098
SNPdbers749465098
MSV3drs749465098
GWAS Ctlgrs749465098
Max Magnitude0
ClinVar
Risk rs749465098(T;T)
Alt rs749465098(T;T)
Reference rs749465098(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18045552C>T
CLNSRC
CLNACC RCV000230123.1,