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rs387907088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907088(G;G)
Make rs387907088(G;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position65328584
GeneMSRB3
is asnp
is mentioned by
dbSNPrs387907088
ebirs387907088
HLIrs387907088
Exacrs387907088
Varsomers387907088
Maprs387907088
PheGenIrs387907088
hapmaprs387907088
1000 genomesrs387907088
hgdprs387907088
ensemblrs387907088
gopubmedrs387907088
geneviewrs387907088
scholarrs387907088
googlers387907088
pharmgkbrs387907088
gwascentralrs387907088
openSNPrs387907088
23andMers387907088
23andMe allrs387907088
SNP Nexus

SNPshotrs387907088
SNPdbers387907088
MSV3drs387907088
GWAS Ctlgrs387907088
Max Magnitude0
ClinVar
Risk rs387907088(G;G)
Alt rs387907088(G;G)
Reference rs387907088(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene MSRB3
CLNDBN Deafness, autosomal recessive 74
Reversed 0
HGVS NC_000012.11:g.65722364T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024049.2,