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

rs875989896

From SNPedia

Orientationplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs875989896(-;-)
Make rs875989896(-;CG)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11102786
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989896
ebirs875989896
HLIrs875989896
Exacrs875989896
Varsomers875989896
Maprs875989896
PheGenIrs875989896
hapmaprs875989896
1000 genomesrs875989896
hgdprs875989896
ensemblrs875989896
gopubmedrs875989896
geneviewrs875989896
scholarrs875989896
googlers875989896
pharmgkbrs875989896
gwascentralrs875989896
openSNPrs875989896
23andMers875989896
23andMe allrs875989896
SNP Nexus

SNPshotrs875989896
SNPdbers875989896
MSV3drs875989896
GWAS Ctlgrs875989896
Max Magnitude0
ClinVar
Risk rs875989896(;)
Alt rs875989896(;)
Reference rs875989896(CG;CG)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11213462_11213463delCG
CLNSRC LDLR @ LOVD
CLNACC RCV000211607.2,