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rs387906300

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906300(C;T)
Make rs387906300(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942567
GeneLCAT
is asnp
is mentioned by
dbSNPrs387906300
ebirs387906300
HLIrs387906300
Exacrs387906300
Varsomers387906300
Maprs387906300
PheGenIrs387906300
hapmaprs387906300
1000 genomesrs387906300
hgdprs387906300
ensemblrs387906300
gopubmedrs387906300
geneviewrs387906300
scholarrs387906300
googlers387906300
pharmgkbrs387906300
gwascentralrs387906300
openSNPrs387906300
23andMers387906300
23andMe allrs387906300
SNP Nexus

SNPshotrs387906300
SNPdbers387906300
MSV3drs387906300
GWAS Ctlgrs387906300
Max Magnitude0
ClinVar
Risk rs387906300(T;T)
Alt rs387906300(T;T)
Reference rs387906300(C;C)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67976470G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003852.3,