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rs727503442

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTGGA;GTGGA) 0 common in clinvar
Make rs727503442(-;-)
Make rs727503442(-;GTGGA)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position43600916
GeneSTRC
is asnp
is mentioned by
dbSNPrs727503442
dbSNP (classic)rs727503442
ClinGenrs727503442
ebirs727503442
HLIrs727503442
Exacrs727503442
Gnomadrs727503442
Varsomers727503442
LitVarrs727503442
Maprs727503442
PheGenIrs727503442
Biobankrs727503442
1000 genomesrs727503442
hgdprs727503442
ensemblrs727503442
geneviewrs727503442
scholarrs727503442
googlers727503442
pharmgkbrs727503442
gwascentralrs727503442
openSNPrs727503442
23andMers727503442
SNPshotrs727503442
SNPdbers727503442
MSV3drs727503442
GWAS Ctlgrs727503442
Max Magnitude0
ClinVar
Risk rs727503442(-;-)
Alt rs727503442(-;-)
Reference Rs727503442(GTGGA;GTGGA)
Significance Pathogenic
Disease Nonsyndromic hearing loss and deafness
Variation info
Gene STRC
CLNDBN Nonsyndromic hearing loss and deafness
Reversed 1
HGVS NC_000015.9:g.43893114_43893118delTCCAC
CLNSRC
CLNACC RCV000151941.1,