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rs373371572

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373371572(C;T)
Make rs373371572(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11116936
GeneLDLR
is asnp
is mentioned by
dbSNPrs373371572
ebirs373371572
HLIrs373371572
Exacrs373371572
Varsomers373371572
Maprs373371572
PheGenIrs373371572
hapmaprs373371572
1000 genomesrs373371572
hgdprs373371572
ensemblrs373371572
gopubmedrs373371572
geneviewrs373371572
scholarrs373371572
googlers373371572
pharmgkbrs373371572
gwascentralrs373371572
openSNPrs373371572
23andMers373371572
23andMe allrs373371572
SNP Nexus

SNPshotrs373371572
SNPdbers373371572
MSV3drs373371572
GWAS Ctlgrs373371572
Max Magnitude0
ClinVar
Risk rs373371572(T;T)
Alt rs373371572(T;T)
Reference rs373371572(C;C)
Significance Probable-Pathogenic
Disease Hypercholesterolaemia Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Hypercholesterolaemia Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11227612C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000148597.1, RCV000237585.1,