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rs794726664

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794726664(C;C)
Make rs794726664(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position67942609
GeneLCAT
is asnp
is mentioned by
dbSNPrs794726664
ebirs794726664
HLIrs794726664
Exacrs794726664
Varsomers794726664
Maprs794726664
PheGenIrs794726664
hapmaprs794726664
1000 genomesrs794726664
hgdprs794726664
ensemblrs794726664
gopubmedrs794726664
geneviewrs794726664
scholarrs794726664
googlers794726664
pharmgkbrs794726664
gwascentralrs794726664
openSNPrs794726664
23andMers794726664
23andMe allrs794726664
SNP Nexus

SNPshotrs794726664
SNPdbers794726664
MSV3drs794726664
GWAS Ctlgrs794726664
Max Magnitude0
ClinVar
Risk rs794726664(C;C)
Alt rs794726664(C;C)
Reference rs794726664(T;T)
Significance Pathogenic
Disease Fish-eye disease
Variation info
Gene LCAT
CLNDBN Fish-eye disease
Reversed 1
HGVS NC_000016.9:g.67976512A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003859.3,