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rs149258390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149258390(C;T)
Make rs149258390(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position65308634
GeneMSRB3
is asnp
is mentioned by
dbSNPrs149258390
ebirs149258390
HLIrs149258390
Exacrs149258390
Varsomers149258390
Maprs149258390
PheGenIrs149258390
hapmaprs149258390
1000 genomesrs149258390
hgdprs149258390
ensemblrs149258390
gopubmedrs149258390
geneviewrs149258390
scholarrs149258390
googlers149258390
pharmgkbrs149258390
gwascentralrs149258390
openSNPrs149258390
23andMers149258390
23andMe allrs149258390
SNP Nexus

SNPshotrs149258390
SNPdbers149258390
MSV3drs149258390
GWAS Ctlgrs149258390
Max Magnitude0
ClinVar
Risk rs149258390(A,T;A,T)
Alt rs149258390(A,T;A,T)
Reference rs149258390(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MSRB3
CLNDBN Deafness, autosomal recessive 74
Reversed 0
HGVS NC_000012.11:g.65702414C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024050.2,