Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122392

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122392(A;A)
Make rs398122392(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position208128258
GeneCRYGC, LOC100507443
is asnp
is mentioned by
dbSNPrs398122392
ebirs398122392
HLIrs398122392
Exacrs398122392
Varsomers398122392
Maprs398122392
PheGenIrs398122392
hapmaprs398122392
1000 genomesrs398122392
hgdprs398122392
ensemblrs398122392
gopubmedrs398122392
geneviewrs398122392
scholarrs398122392
googlers398122392
pharmgkbrs398122392
gwascentralrs398122392
openSNPrs398122392
23andMers398122392
23andMe allrs398122392
SNP Nexus

SNPshotrs398122392
SNPdbers398122392
MSV3drs398122392
GWAS Ctlgrs398122392
Max Magnitude0
ClinVar
Risk rs398122392(A,C,T;A,C,T)
Alt rs398122392(A,C,T;A,C,T)
Reference rs398122392(G;G)
Significance Pathogenic
Disease Cataract
Variation info
Gene CRYGC LOC100507443
CLNDBN Cataract, coppock-like
Reversed 1
HGVS NC_000002.11:g.208992982C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056309.23,