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rs794726663

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794726663(-;A)
Make rs794726663(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position67940029
GeneLCAT
is asnp
is mentioned by
dbSNPrs794726663
ClinGenrs794726663
ebirs794726663
HLIrs794726663
Exacrs794726663
Varsomers794726663
Maprs794726663
PheGenIrs794726663
hapmaprs794726663
1000 genomesrs794726663
hgdprs794726663
ensemblrs794726663
gopubmedrs794726663
geneviewrs794726663
scholarrs794726663
googlers794726663
pharmgkbrs794726663
gwascentralrs794726663
openSNPrs794726663
23andMers794726663
23andMe allrs794726663
SNP Nexus

SNPshotrs794726663
SNPdbers794726663
MSV3drs794726663
GWAS Ctlgrs794726663
Max Magnitude0
ClinVar
Risk rs794726663(A;A)
Alt rs794726663(A;A)
Reference Rs794726663(;)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67973933dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000003854.3,