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rs727505074

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727505074(-;-)
Make rs727505074(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position43610326
GeneSTRC
is asnp
is mentioned by
dbSNPrs727505074
ebirs727505074
HLIrs727505074
Exacrs727505074
Varsomers727505074
Maprs727505074
PheGenIrs727505074
hapmaprs727505074
1000 genomesrs727505074
hgdprs727505074
ensemblrs727505074
gopubmedrs727505074
geneviewrs727505074
scholarrs727505074
googlers727505074
pharmgkbrs727505074
gwascentralrs727505074
openSNPrs727505074
23andMers727505074
23andMe allrs727505074
SNP Nexus

SNPshotrs727505074
SNPdbers727505074
MSV3drs727505074
GWAS Ctlgrs727505074
Max Magnitude0
ClinVar
Risk rs727505074(;)
Alt rs727505074(;)
Reference rs727505074(T;T)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene STRC
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000015.9:g.43902524delA
CLNSRC
CLNACC RCV000156514.1,