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rs864309694

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309694(C;C)
Make rs864309694(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position20143282
GeneGJA3
is asnp
is mentioned by
dbSNPrs864309694
ebirs864309694
HLIrs864309694
Exacrs864309694
Varsomers864309694
Maprs864309694
PheGenIrs864309694
hapmaprs864309694
1000 genomesrs864309694
hgdprs864309694
ensemblrs864309694
gopubmedrs864309694
geneviewrs864309694
scholarrs864309694
googlers864309694
pharmgkbrs864309694
gwascentralrs864309694
openSNPrs864309694
23andMers864309694
23andMe allrs864309694
SNP Nexus

SNPshotrs864309694
SNPdbers864309694
MSV3drs864309694
GWAS Ctlgrs864309694
Max Magnitude0
ClinVar
Risk rs864309694(C;C)
Alt rs864309694(C;C)
Reference rs864309694(G;G)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene GJA3
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000013.10:g.20717421C>G
CLNSRC
CLNACC RCV000203361.1,