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rs774312182

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774312182(A;A)
Make rs774312182(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position43604720
GeneSTRC
is asnp
is mentioned by
dbSNPrs774312182
ebirs774312182
HLIrs774312182
Exacrs774312182
Varsomers774312182
Maprs774312182
PheGenIrs774312182
hapmaprs774312182
1000 genomesrs774312182
hgdprs774312182
ensemblrs774312182
gopubmedrs774312182
geneviewrs774312182
scholarrs774312182
googlers774312182
pharmgkbrs774312182
gwascentralrs774312182
openSNPrs774312182
23andMers774312182
23andMe allrs774312182
SNP Nexus

SNPshotrs774312182
SNPdbers774312182
MSV3drs774312182
GWAS Ctlgrs774312182
Max Magnitude0
ClinVar
Risk rs774312182(A;A)
Alt rs774312182(A;A)
Reference rs774312182(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene STRC
CLNDBN Deafness, autosomal dominant 16
Reversed 0
HGVS NC_000015.9:g.43896918G>A
CLNSRC
CLNACC RCV000225080.1,