Rs121908050

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908050(C;T)
Make rs121908050(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942754
GeneLCAT
is asnp
is mentioned by
dbSNPrs121908050
PheGenIrs121908050
nextbiors121908050
hapmaprs121908050
1000 genomesrs121908050
hgdprs121908050
ensemblrs121908050
gopubmedrs121908050
geneviewrs121908050
scholarrs121908050
googlers121908050
pharmgkbrs121908050
gwascentralrs121908050
openSNPrs121908050
23andMers121908050
23andMe allrs121908050
SNP Nexus

SNPshotrs121908050
SNPdbers121908050
MSV3drs121908050
Max Magnitude0
OMIM606967
Desc
Variant0005
Relatedalso
OMIM606967
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908050(T;T)
Alt rs121908050(T;T)
Reference rs121908050(C;C)
Significance Pathogenic
Disease Fish-eye disease
Variation info
Gene LCAT
CLNDBN Fish-eye disease
Reversed 1
HGVS NC_000016.9:g.67976657G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003845.1,