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rs864309692

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309692(C;T)
Make rs864309692(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position79598988
GeneLOC101928230, MAF
is asnp
is mentioned by
dbSNPrs864309692
ebirs864309692
HLIrs864309692
Exacrs864309692
Varsomers864309692
Maprs864309692
PheGenIrs864309692
hapmaprs864309692
1000 genomesrs864309692
hgdprs864309692
ensemblrs864309692
gopubmedrs864309692
geneviewrs864309692
scholarrs864309692
googlers864309692
pharmgkbrs864309692
gwascentralrs864309692
openSNPrs864309692
23andMers864309692
23andMe allrs864309692
SNP Nexus

SNPshotrs864309692
SNPdbers864309692
MSV3drs864309692
GWAS Ctlgrs864309692
Max Magnitude0
ClinVar
Risk rs864309692(T;T)
Alt rs864309692(T;T)
Reference rs864309692(C;C)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene MAF LOC101928230
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000016.9:g.79632885G>A
CLNSRC
CLNACC RCV000203395.1,