Rs121908057

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908057(A;G)
Make rs121908057(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942731
GeneLCAT
is asnp
is mentioned by
dbSNPrs121908057
Exacrs121908057
PheGenIrs121908057
nextbiors121908057
hapmaprs121908057
1000 genomesrs121908057
hgdprs121908057
ensemblrs121908057
gopubmedrs121908057
geneviewrs121908057
scholarrs121908057
googlers121908057
pharmgkbrs121908057
gwascentralrs121908057
openSNPrs121908057
23andMers121908057
23andMe allrs121908057
SNP Nexus

SNPshotrs121908057
SNPdbers121908057
MSV3drs121908057
Max Magnitude0
OMIM606967
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121908057(G;G)
Alt rs121908057(G;G)
Reference rs121908057(A;A)
Significance Pathogenic
Disease Fish-eye disease
Variation info
Gene LCAT
CLNDBN Fish-eye disease
Reversed 1
HGVS NC_000016.9:g.67976634T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003858.1,