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rs121908967

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908967(A;T)
Make rs121908967(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18151859
GeneMYO15A
is asnp
is mentioned by
dbSNPrs121908967
ebirs121908967
HLIrs121908967
Exacrs121908967
Varsomers121908967
Maprs121908967
PheGenIrs121908967
hapmaprs121908967
1000 genomesrs121908967
hgdprs121908967
ensemblrs121908967
gopubmedrs121908967
geneviewrs121908967
scholarrs121908967
googlers121908967
pharmgkbrs121908967
gwascentralrs121908967
openSNPrs121908967
23andMers121908967
23andMe allrs121908967
SNP Nexus

SNPshotrs121908967
SNPdbers121908967
MSV3drs121908967
GWAS Ctlgrs121908967
Max Magnitude0
OMIM602666
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908967(T;T)
Alt rs121908967(T;T)
Reference rs121908967(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18055173A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007367.2,