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rs864309693

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309693(C;T)
Make rs864309693(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position56454517
GeneMIP
is asnp
is mentioned by
dbSNPrs864309693
ebirs864309693
HLIrs864309693
Exacrs864309693
Varsomers864309693
Maprs864309693
PheGenIrs864309693
hapmaprs864309693
1000 genomesrs864309693
hgdprs864309693
ensemblrs864309693
gopubmedrs864309693
geneviewrs864309693
scholarrs864309693
googlers864309693
pharmgkbrs864309693
gwascentralrs864309693
openSNPrs864309693
23andMers864309693
23andMe allrs864309693
SNP Nexus

SNPshotrs864309693
SNPdbers864309693
MSV3drs864309693
GWAS Ctlgrs864309693
Max Magnitude0
ClinVar
Risk rs864309693(T;T)
Alt rs864309693(T;T)
Reference rs864309693(C;C)
Significance Pathogenic
Disease Congenital cataract
Variation info
Gene MIP
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000012.11:g.56848301G>A
CLNSRC
CLNACC RCV000203320.1,