Rs121908054

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908054(A;A)
Make rs121908054(A;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67940400
GeneLCAT
is asnp
is mentioned by
dbSNPrs121908054
Exacrs121908054
PheGenIrs121908054
nextbiors121908054
hapmaprs121908054
1000 genomesrs121908054
hgdprs121908054
ensemblrs121908054
gopubmedrs121908054
geneviewrs121908054
scholarrs121908054
googlers121908054
pharmgkbrs121908054
gwascentralrs121908054
openSNPrs121908054
23andMers121908054
23andMe allrs121908054
SNP Nexus

SNPshotrs121908054
SNPdbers121908054
MSV3drs121908054
Max Magnitude0
OMIM606967
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908054(A;A)
Alt rs121908054(A;A)
Reference rs121908054(T;T)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67974303A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003850.1,