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rs371513959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371513959(A;A)
Make rs371513959(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position43604384
GeneSTRC
is asnp
is mentioned by
dbSNPrs371513959
dbSNP (old)rs371513959
ClinGenrs371513959
ebirs371513959
HLIrs371513959
Exacrs371513959
Varsomers371513959
Maprs371513959
PheGenIrs371513959
Biobankrs371513959
1000 genomesrs371513959
hgdprs371513959
ensemblrs371513959
gopubmedrs371513959
geneviewrs371513959
scholarrs371513959
googlers371513959
pharmgkbrs371513959
gwascentralrs371513959
openSNPrs371513959
23andMers371513959
23andMe allrs371513959
SNP Nexus

SNPshotrs371513959
SNPdbers371513959
MSV3drs371513959
GWAS Ctlgrs371513959
Max Magnitude0
ClinVar
Risk rs371513959(A;A)
Alt rs371513959(A;A)
Reference Rs371513959(C;C)
Significance Pathogenic
Disease Nonsyndromic hearing loss and deafness
Variation info
Gene STRC
CLNDBN Nonsyndromic hearing loss and deafness
Reversed 0
HGVS NC_000015.9:g.43896582C>A
CLNSRC
CLNACC RCV000151949.1,