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rs121909595

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909595(C;T)
Make rs121909595(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position208124321
GeneCRYGD, ZNF224
is asnp
is mentioned by
dbSNPrs121909595
ebirs121909595
HLIrs121909595
Exacrs121909595
Varsomers121909595
Maprs121909595
PheGenIrs121909595
hapmaprs121909595
1000 genomesrs121909595
hgdprs121909595
ensemblrs121909595
gopubmedrs121909595
geneviewrs121909595
scholarrs121909595
googlers121909595
pharmgkbrs121909595
gwascentralrs121909595
openSNPrs121909595
23andMers121909595
23andMe allrs121909595
SNP Nexus

SNPshotrs121909595
SNPdbers121909595
MSV3drs121909595
GWAS Ctlgrs121909595
Max Magnitude0
OMIM123690
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909595(T;T)
Alt rs121909595(T;T)
Reference rs121909595(C;C)
Significance Pathogenic
Disease Cataract 4
Variation info
Gene LOC100507443 CRYGD
CLNDBN Cataract 4
Reversed 1
HGVS NC_000002.11:g.208989045G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018445.30,