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rs727503443

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503443(C;C)
Make rs727503443(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position43603362
GeneSTRC
is asnp
is mentioned by
dbSNPrs727503443
ebirs727503443
HLIrs727503443
Exacrs727503443
Varsomers727503443
Maprs727503443
PheGenIrs727503443
hapmaprs727503443
1000 genomesrs727503443
hgdprs727503443
ensemblrs727503443
gopubmedrs727503443
geneviewrs727503443
scholarrs727503443
googlers727503443
pharmgkbrs727503443
gwascentralrs727503443
openSNPrs727503443
23andMers727503443
23andMe allrs727503443
SNP Nexus

SNPshotrs727503443
SNPdbers727503443
MSV3drs727503443
GWAS Ctlgrs727503443
Max Magnitude0
ClinVar
Risk rs727503443(C;C)
Alt rs727503443(C;C)
Reference rs727503443(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene STRC
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000015.9:g.43895560C>G
CLNSRC
CLNACC RCV000151947.2,