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rs137853924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853924(G;T)
Make rs137853924(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position208128343
GeneCRYGC, LOC100507443
is asnp
is mentioned by
dbSNPrs137853924
ebirs137853924
HLIrs137853924
Exacrs137853924
Varsomers137853924
Maprs137853924
PheGenIrs137853924
hapmaprs137853924
1000 genomesrs137853924
hgdprs137853924
ensemblrs137853924
gopubmedrs137853924
geneviewrs137853924
scholarrs137853924
googlers137853924
pharmgkbrs137853924
gwascentralrs137853924
openSNPrs137853924
23andMers137853924
23andMe allrs137853924
SNP Nexus

SNPshotrs137853924
SNPdbers137853924
MSV3drs137853924
GWAS Ctlgrs137853924
Max Magnitude0
ClinVar
Risk rs137853924(T;T)
Alt rs137853924(T;T)
Reference rs137853924(G;G)
Significance Pathogenic
Disease Cataract
Variation info
Gene CRYGC LOC100507443
CLNDBN Cataract, coppock-like
Reversed 1
HGVS NC_000002.11:g.208993067C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000056311.23,