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rs864309695

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309695(C;T)
Make rs864309695(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position79599023
GeneLOC101928230, MAF
is asnp
is mentioned by
dbSNPrs864309695
ebirs864309695
HLIrs864309695
Exacrs864309695
Varsomers864309695
Maprs864309695
PheGenIrs864309695
hapmaprs864309695
1000 genomesrs864309695
hgdprs864309695
ensemblrs864309695
gopubmedrs864309695
geneviewrs864309695
scholarrs864309695
googlers864309695
pharmgkbrs864309695
gwascentralrs864309695
openSNPrs864309695
23andMers864309695
23andMe allrs864309695
SNP Nexus

SNPshotrs864309695
SNPdbers864309695
MSV3drs864309695
GWAS Ctlgrs864309695
Max Magnitude0
ClinVar
Risk rs864309695(T;T)
Alt rs864309695(T;T)
Reference rs864309695(C;C)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene MAF LOC101928230
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000016.9:g.79632920G>A
CLNSRC
CLNACC RCV000203408.1,