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rs875989937

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989937(-;-)
Make rs875989937(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11120409
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989937
ebirs875989937
HLIrs875989937
Exacrs875989937
Varsomers875989937
Maprs875989937
PheGenIrs875989937
hapmaprs875989937
1000 genomesrs875989937
hgdprs875989937
ensemblrs875989937
gopubmedrs875989937
geneviewrs875989937
scholarrs875989937
googlers875989937
pharmgkbrs875989937
gwascentralrs875989937
openSNPrs875989937
23andMers875989937
23andMe allrs875989937
SNP Nexus

SNPshotrs875989937
SNPdbers875989937
MSV3drs875989937
GWAS Ctlgrs875989937
Max Magnitude0
ClinVar
Risk rs875989937(;)
Alt rs875989937(;)
Reference rs875989937(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11231085delG
CLNSRC
CLNACC RCV000211640.1,