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

rs869320649

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869320649(-;-)
Make rs869320649(-;TG)
Make rs869320649(TG;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105566
GeneLDLR
is asnp
is mentioned by
dbSNPrs869320649
ebirs869320649
HLIrs869320649
Exacrs869320649
Varsomers869320649
Maprs869320649
PheGenIrs869320649
hapmaprs869320649
1000 genomesrs869320649
hgdprs869320649
ensemblrs869320649
gopubmedrs869320649
geneviewrs869320649
scholarrs869320649
googlers869320649
pharmgkbrs869320649
gwascentralrs869320649
openSNPrs869320649
23andMers869320649
23andMe allrs869320649
SNP Nexus

SNPshotrs869320649
SNPdbers869320649
MSV3drs869320649
GWAS Ctlgrs869320649
Max Magnitude0
ClinVar
Risk rs869320649(TG;TG)
Alt rs869320649(TG;TG)
Reference rs869320649(;)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11216242_11216243insTG
CLNSRC
CLNACC RCV000210842.1,