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rs864309701

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864309701(-;G)
Make rs864309701(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position208121749
GeneCRYGD, LOC100507443
is asnp
is mentioned by
dbSNPrs864309701
dbSNP (old)rs864309701
ClinGenrs864309701
ebirs864309701
HLIrs864309701
Exacrs864309701
Gnomadrs864309701
Varsomers864309701
Maprs864309701
PheGenIrs864309701
Biobankrs864309701
1000 genomesrs864309701
hgdprs864309701
ensemblrs864309701
gopubmedrs864309701
geneviewrs864309701
scholarrs864309701
googlers864309701
pharmgkbrs864309701
gwascentralrs864309701
openSNPrs864309701
23andMers864309701
23andMe allrs864309701
SNP Nexus

SNPshotrs864309701
SNPdbers864309701
MSV3drs864309701
GWAS Ctlgrs864309701
Max Magnitude0
ClinVar
Risk rs864309701(G;G)
Alt rs864309701(G;G)
Reference Rs864309701(-;-)
Significance Pathogenic
Disease Congenital cataract
Variation info
Gene CRYGD LOC100507443
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000002.11:g.208986474dupC
CLNSRC
CLNACC RCV000203375.1,