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rs587778872

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778872(C;T)
Make rs587778872(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position208128231
GeneCRYGC, LOC100507443
is asnp
is mentioned by
dbSNPrs587778872
ebirs587778872
HLIrs587778872
Exacrs587778872
Varsomers587778872
Maprs587778872
PheGenIrs587778872
hapmaprs587778872
1000 genomesrs587778872
hgdprs587778872
ensemblrs587778872
gopubmedrs587778872
geneviewrs587778872
scholarrs587778872
googlers587778872
pharmgkbrs587778872
gwascentralrs587778872
openSNPrs587778872
23andMers587778872
23andMe allrs587778872
SNP Nexus

SNPshotrs587778872
SNPdbers587778872
MSV3drs587778872
GWAS Ctlgrs587778872
Max Magnitude0
ClinVar
Risk rs587778872(T;T)
Alt rs587778872(T;T)
Reference rs587778872(C;C)
Significance Pathogenic
Disease Cataract Congenital cataract
Variation info
Gene CRYGC LOC100507443
CLNDBN Cataract, coppock-like Congenital cataract
Reversed 1
HGVS NC_000002.11:g.208992955G>A
CLNSRC
CLNACC RCV000059346.2, RCV000203402.1,