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rs752951310

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752951310(C;C)
Make rs752951310(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11111598
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs752951310
ebirs752951310
HLIrs752951310
Exacrs752951310
Varsomers752951310
Maprs752951310
PheGenIrs752951310
hapmaprs752951310
1000 genomesrs752951310
hgdprs752951310
ensemblrs752951310
gopubmedrs752951310
geneviewrs752951310
scholarrs752951310
googlers752951310
pharmgkbrs752951310
gwascentralrs752951310
openSNPrs752951310
23andMers752951310
23andMe allrs752951310
SNP Nexus

SNPshotrs752951310
SNPdbers752951310
MSV3drs752951310
GWAS Ctlgrs752951310
Max Magnitude0
ClinVar
Risk rs752951310(C;C)
Alt rs752951310(C;C)
Reference rs752951310(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222274G>T
CLNSRC LDLR @ LOVD
CLNACC RCV000238258.1,