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rs727503062

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503062(A;A)
Make rs727503062(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position3585719
GeneGIPC3
is asnp
is mentioned by
dbSNPrs727503062
ebirs727503062
HLIrs727503062
Exacrs727503062
Varsomers727503062
Maprs727503062
PheGenIrs727503062
hapmaprs727503062
1000 genomesrs727503062
hgdprs727503062
ensemblrs727503062
gopubmedrs727503062
geneviewrs727503062
scholarrs727503062
googlers727503062
pharmgkbrs727503062
gwascentralrs727503062
openSNPrs727503062
23andMers727503062
23andMe allrs727503062
SNP Nexus

SNPshotrs727503062
SNPdbers727503062
MSV3drs727503062
GWAS Ctlgrs727503062
Max Magnitude0
ClinVar
Risk rs727503062(A;A)
Alt rs727503062(A;A)
Reference rs727503062(C;C)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene GIPC3
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000019.9:g.3585717C>A
CLNSRC
CLNACC RCV000150720.1,