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

rs151207122

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151207122(C;T)
Make rs151207122(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11107481
GeneLDLR
is asnp
is mentioned by
dbSNPrs151207122
ebirs151207122
HLIrs151207122
Exacrs151207122
Varsomers151207122
Maprs151207122
PheGenIrs151207122
hapmaprs151207122
1000 genomesrs151207122
hgdprs151207122
ensemblrs151207122
gopubmedrs151207122
geneviewrs151207122
scholarrs151207122
googlers151207122
pharmgkbrs151207122
gwascentralrs151207122
openSNPrs151207122
23andMers151207122
23andMe allrs151207122
SNP Nexus

SNPshotrs151207122
SNPdbers151207122
MSV3drs151207122
GWAS Ctlgrs151207122
Max Magnitude0
ClinVar
Risk rs151207122(T;T)
Alt rs151207122(T;T)
Reference rs151207122(C;C)
Significance Probable-Pathogenic
Disease Hypercholesterolaemia Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Hypercholesterolaemia Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11218157C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000148588.1, RCV000238462.1,