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rs121908968

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908968(C;T)
Make rs121908968(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18124558
GeneMYO15A
is asnp
is mentioned by
dbSNPrs121908968
ebirs121908968
HLIrs121908968
Exacrs121908968
Varsomers121908968
Maprs121908968
PheGenIrs121908968
hapmaprs121908968
1000 genomesrs121908968
hgdprs121908968
ensemblrs121908968
gopubmedrs121908968
geneviewrs121908968
scholarrs121908968
googlers121908968
pharmgkbrs121908968
gwascentralrs121908968
openSNPrs121908968
23andMers121908968
23andMe allrs121908968
SNP Nexus

SNPshotrs121908968
SNPdbers121908968
MSV3drs121908968
GWAS Ctlgrs121908968
Max Magnitude0
OMIM602666
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908968(T;T)
Alt rs121908968(T;T)
Reference rs121908968(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18027872C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007368.2,