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rs786200882

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200882(-;-)
Make rs786200882(-;C)
Make rs786200882(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position43611297
GeneSTRC
is asnp
is mentioned by
dbSNPrs786200882
ebirs786200882
HLIrs786200882
Exacrs786200882
Varsomers786200882
Maprs786200882
PheGenIrs786200882
hapmaprs786200882
1000 genomesrs786200882
hgdprs786200882
ensemblrs786200882
gopubmedrs786200882
geneviewrs786200882
scholarrs786200882
googlers786200882
pharmgkbrs786200882
gwascentralrs786200882
openSNPrs786200882
23andMers786200882
23andMe allrs786200882
SNP Nexus

SNPshotrs786200882
SNPdbers786200882
MSV3drs786200882
GWAS Ctlgrs786200882
Max Magnitude0
ClinVar
Risk rs786200882(C;C)
Alt rs786200882(C;C)
Reference rs786200882(;)
Significance Pathogenic
Disease Deafness
Variation info
Gene STRC
CLNDBN Deafness, autosomal recessive 16
Reversed 1
HGVS NC_000015.9:g.43903496dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004591.3,