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rs864309687

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309687(C;T)
Make rs864309687(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position20143029
GeneGJA3
is asnp
is mentioned by
dbSNPrs864309687
ebirs864309687
HLIrs864309687
Exacrs864309687
Varsomers864309687
Maprs864309687
PheGenIrs864309687
hapmaprs864309687
1000 genomesrs864309687
hgdprs864309687
ensemblrs864309687
gopubmedrs864309687
geneviewrs864309687
scholarrs864309687
googlers864309687
pharmgkbrs864309687
gwascentralrs864309687
openSNPrs864309687
23andMers864309687
23andMe allrs864309687
SNP Nexus

SNPshotrs864309687
SNPdbers864309687
MSV3drs864309687
GWAS Ctlgrs864309687
Max Magnitude0
ClinVar
Risk rs864309687(T;T)
Alt rs864309687(T;T)
Reference rs864309687(C;C)
Significance Pathogenic
Disease Congenital cataract
Variation info
Gene GJA3
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000013.10:g.20717168G>A
CLNSRC
CLNACC RCV000203373.1,