Have questions? Visit https://www.reddit.com/r/SNPedia

rs370018159

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370018159(A;A)
Make rs370018159(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11123248
GeneLDLR
is asnp
is mentioned by
dbSNPrs370018159
ebirs370018159
HLIrs370018159
Exacrs370018159
Varsomers370018159
Maprs370018159
PheGenIrs370018159
hapmaprs370018159
1000 genomesrs370018159
hgdprs370018159
ensemblrs370018159
gopubmedrs370018159
geneviewrs370018159
scholarrs370018159
googlers370018159
pharmgkbrs370018159
gwascentralrs370018159
openSNPrs370018159
23andMers370018159
23andMe allrs370018159
SNP Nexus

SNPshotrs370018159
SNPdbers370018159
MSV3drs370018159
GWAS Ctlgrs370018159
Max Magnitude0
ClinVar
Risk rs370018159(A;A)
Alt rs370018159(A;A)
Reference rs370018159(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11233924C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000237494.1,