Rs121908051

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908051(C;T)
Make rs121908051(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67944001
GeneLCAT, SLC12A4
is asnp
is mentioned by
dbSNPrs121908051
PheGenIrs121908051
nextbiors121908051
hapmaprs121908051
1000 genomesrs121908051
hgdprs121908051
ensemblrs121908051
gopubmedrs121908051
geneviewrs121908051
scholarrs121908051
googlers121908051
pharmgkbrs121908051
gwascentralrs121908051
openSNPrs121908051
23andMers121908051
23andMe allrs121908051
SNP Nexus

SNPshotrs121908051
SNPdbers121908051
MSV3drs121908051
Max Magnitude0
OMIM606967
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908051(T;T)
Alt rs121908051(T;T)
Reference rs121908051(C;C)
Significance Pathogenic
Disease Fish-eye disease
Variation info
Gene LCAT SLC12A4
CLNDBN Fish-eye disease
Reversed 1
HGVS NC_000016.9:g.67977904G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003847.1,