Rs121908055

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908055(A;A)
Make rs121908055(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942967
GeneLCAT
is asnp
is mentioned by
dbSNPrs121908055
Exacrs121908055
PheGenIrs121908055
nextbiors121908055
hapmaprs121908055
1000 genomesrs121908055
hgdprs121908055
ensemblrs121908055
gopubmedrs121908055
geneviewrs121908055
scholarrs121908055
googlers121908055
pharmgkbrs121908055
gwascentralrs121908055
openSNPrs121908055
23andMers121908055
23andMe allrs121908055
SNP Nexus

SNPshotrs121908055
SNPdbers121908055
MSV3drs121908055
OMIM606967
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121908055(A;A)
Alt rs121908055(A;A)
Reference rs121908055(C;C)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67976870G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003856.1,