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rs377480477

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377480477(A;A)
Make rs377480477(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position43603385
GeneSTRC
is asnp
is mentioned by
dbSNPrs377480477
ebirs377480477
HLIrs377480477
Exacrs377480477
Varsomers377480477
Maprs377480477
PheGenIrs377480477
hapmaprs377480477
1000 genomesrs377480477
hgdprs377480477
ensemblrs377480477
gopubmedrs377480477
geneviewrs377480477
scholarrs377480477
googlers377480477
pharmgkbrs377480477
gwascentralrs377480477
openSNPrs377480477
23andMers377480477
23andMe allrs377480477
SNP Nexus

SNPshotrs377480477
SNPdbers377480477
MSV3drs377480477
GWAS Ctlgrs377480477
Max Magnitude0
ClinVar
Risk rs377480477(A;A)
Alt rs377480477(A;A)
Reference rs377480477(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene STRC
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000015.9:g.43895583G>A
CLNSRC
CLNACC RCV000156556.2,