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rs387906966

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906966(C;T)
Make rs387906966(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position45967788
GeneFYCO1
is asnp
is mentioned by
dbSNPrs387906966
ebirs387906966
HLIrs387906966
Exacrs387906966
Varsomers387906966
Maprs387906966
PheGenIrs387906966
hapmaprs387906966
1000 genomesrs387906966
hgdprs387906966
ensemblrs387906966
gopubmedrs387906966
geneviewrs387906966
scholarrs387906966
googlers387906966
pharmgkbrs387906966
gwascentralrs387906966
openSNPrs387906966
23andMers387906966
23andMe allrs387906966
SNP Nexus

SNPshotrs387906966
SNPdbers387906966
MSV3drs387906966
GWAS Ctlgrs387906966
Max Magnitude0
ClinVar
Risk rs387906966(T;T)
Alt rs387906966(T;T)
Reference rs387906966(C;C)
Significance Pathogenic
Disease Cataract
Variation info
Gene FYCO1
CLNDBN Cataract, autosomal recessive congenital 2
Reversed 1
HGVS NC_000003.11:g.46009280G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023625.3,