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rs869320648

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320648(A;A)
Make rs869320648(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105261
GeneLDLR
is asnp
is mentioned by
dbSNPrs869320648
ebirs869320648
HLIrs869320648
Exacrs869320648
Varsomers869320648
Maprs869320648
PheGenIrs869320648
hapmaprs869320648
1000 genomesrs869320648
hgdprs869320648
ensemblrs869320648
gopubmedrs869320648
geneviewrs869320648
scholarrs869320648
googlers869320648
pharmgkbrs869320648
gwascentralrs869320648
openSNPrs869320648
23andMers869320648
23andMe allrs869320648
SNP Nexus

SNPshotrs869320648
SNPdbers869320648
MSV3drs869320648
GWAS Ctlgrs869320648
Max Magnitude0
ClinVar
Risk rs869320648(A;A)
Alt rs869320648(A;A)
Reference rs869320648(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11215937G>A
CLNSRC
CLNACC RCV000210835.1,