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rs727503444

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503444(C;T)
Make rs727503444(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position43608091
GeneSTRC
is asnp
is mentioned by
dbSNPrs727503444
ebirs727503444
HLIrs727503444
Exacrs727503444
Varsomers727503444
Maprs727503444
PheGenIrs727503444
hapmaprs727503444
1000 genomesrs727503444
hgdprs727503444
ensemblrs727503444
gopubmedrs727503444
geneviewrs727503444
scholarrs727503444
googlers727503444
pharmgkbrs727503444
gwascentralrs727503444
openSNPrs727503444
23andMers727503444
23andMe allrs727503444
SNP Nexus

SNPshotrs727503444
SNPdbers727503444
MSV3drs727503444
GWAS Ctlgrs727503444
Max Magnitude0
ClinVar
Risk rs727503444(T;T)
Alt rs727503444(T;T)
Reference rs727503444(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene STRC
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000015.9:g.43900289G>A
CLNSRC
CLNACC RCV000151954.2,