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rs875989925

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989925(A;A)
Make rs875989925(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11116192
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989925
ebirs875989925
HLIrs875989925
Exacrs875989925
Varsomers875989925
Maprs875989925
PheGenIrs875989925
hapmaprs875989925
1000 genomesrs875989925
hgdprs875989925
ensemblrs875989925
gopubmedrs875989925
geneviewrs875989925
scholarrs875989925
googlers875989925
pharmgkbrs875989925
gwascentralrs875989925
openSNPrs875989925
23andMers875989925
23andMe allrs875989925
SNP Nexus

SNPshotrs875989925
SNPdbers875989925
MSV3drs875989925
GWAS Ctlgrs875989925
Max Magnitude0
ClinVar
Risk rs875989925(A;A)
Alt rs875989925(A;A)
Reference rs875989925(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11226868G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000211573.2,