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rs184435771

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs184435771(A;A)
Make rs184435771(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18154714
GeneLOC105371568, MYO15A
is asnp
is mentioned by
dbSNPrs184435771
ebirs184435771
HLIrs184435771
Exacrs184435771
Varsomers184435771
Maprs184435771
PheGenIrs184435771
hapmaprs184435771
1000 genomesrs184435771
hgdprs184435771
ensemblrs184435771
gopubmedrs184435771
geneviewrs184435771
scholarrs184435771
googlers184435771
pharmgkbrs184435771
gwascentralrs184435771
openSNPrs184435771
23andMers184435771
23andMe allrs184435771
SNP Nexus

SNPshotrs184435771
SNPdbers184435771
MSV3drs184435771
GWAS Ctlgrs184435771
Max Magnitude0
ClinVar
Risk rs184435771(A;A)
Alt rs184435771(A;A)
Reference rs184435771(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness Deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18058028G>A
CLNSRC
CLNACC RCV000218811.1, RCV000225017.1,