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rs144451841

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs144451841(C;T)
Make rs144451841(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position111910331
GeneCRYAB
is asnp
is mentioned by
dbSNPrs144451841
ebirs144451841
HLIrs144451841
Exacrs144451841
Varsomers144451841
Maprs144451841
PheGenIrs144451841
hapmaprs144451841
1000 genomesrs144451841
hgdprs144451841
ensemblrs144451841
gopubmedrs144451841
geneviewrs144451841
scholarrs144451841
googlers144451841
pharmgkbrs144451841
gwascentralrs144451841
openSNPrs144451841
23andMers144451841
23andMe allrs144451841
SNP Nexus

SNPshotrs144451841
SNPdbers144451841
MSV3drs144451841
GWAS Ctlgrs144451841
Max Magnitude0
ClinVar
Risk rs144451841(T;T)
Alt rs144451841(T;T)
Reference rs144451841(C;C)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene CRYAB
CLNDBN Congenital cataract
Reversed 0
HGVS NC_000011.9:g.111781055C>A
CLNSRC
CLNACC RCV000203405.1,