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rs267607211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607211(C;C)
Make rs267607211(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942686
GeneLCAT
is asnp
is mentioned by
dbSNPrs267607211
ebirs267607211
HLIrs267607211
Exacrs267607211
Varsomers267607211
Maprs267607211
PheGenIrs267607211
hapmaprs267607211
1000 genomesrs267607211
hgdprs267607211
ensemblrs267607211
gopubmedrs267607211
geneviewrs267607211
scholarrs267607211
googlers267607211
pharmgkbrs267607211
gwascentralrs267607211
openSNPrs267607211
23andMers267607211
23andMe allrs267607211
SNP Nexus

SNPshotrs267607211
SNPdbers267607211
MSV3drs267607211
GWAS Ctlgrs267607211
Max Magnitude0
ClinVar
Risk rs267607211(C;C)
Alt rs267607211(C;C)
Reference rs267607211(T;T)
Significance Pathogenic
Disease Norum disease
Variation info
Gene LCAT
CLNDBN Norum disease
Reversed 1
HGVS NC_000016.9:g.67976589A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003841.3,