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rs121908048

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908048(A;A)
Make rs121908048(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position67940276
GeneLCAT
is asnp
is mentioned by
dbSNPrs121908048
ebirs121908048
HLIrs121908048
Exacrs121908048
Varsomers121908048
Maprs121908048
PheGenIrs121908048
hapmaprs121908048
1000 genomesrs121908048
hgdprs121908048
ensemblrs121908048
gopubmedrs121908048
geneviewrs121908048
scholarrs121908048
googlers121908048
pharmgkbrs121908048
gwascentralrs121908048
openSNPrs121908048
23andMers121908048
23andMe allrs121908048
SNP Nexus

SNPshotrs121908048
SNPdbers121908048
MSV3drs121908048
GWAS Ctlgrs121908048
Max Magnitude0
OMIM606967
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908048(A;A)
Alt rs121908048(A;A)
Reference rs121908048(G;G)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67974179C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003842.3,