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

rs146675823

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146675823(A;A)
Make rs146675823(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11102706
GeneLDLR
is asnp
is mentioned by
dbSNPrs146675823
ebirs146675823
HLIrs146675823
Exacrs146675823
Varsomers146675823
Maprs146675823
PheGenIrs146675823
hapmaprs146675823
1000 genomesrs146675823
hgdprs146675823
ensemblrs146675823
gopubmedrs146675823
geneviewrs146675823
scholarrs146675823
googlers146675823
pharmgkbrs146675823
gwascentralrs146675823
openSNPrs146675823
23andMers146675823
23andMe allrs146675823
SNP Nexus

SNPshotrs146675823
SNPdbers146675823
MSV3drs146675823
GWAS Ctlgrs146675823
Max Magnitude0
ClinVar
Risk rs146675823(A,T;A,T)
Alt rs146675823(A,T;A,T)
Reference rs146675823(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11213382G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000238230.1,