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rs768430352

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768430352(A;A)
Make rs768430352(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11111556
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs768430352
ebirs768430352
HLIrs768430352
Exacrs768430352
Varsomers768430352
Maprs768430352
PheGenIrs768430352
hapmaprs768430352
1000 genomesrs768430352
hgdprs768430352
ensemblrs768430352
gopubmedrs768430352
geneviewrs768430352
scholarrs768430352
googlers768430352
pharmgkbrs768430352
gwascentralrs768430352
openSNPrs768430352
23andMers768430352
23andMe allrs768430352
SNP Nexus

SNPshotrs768430352
SNPdbers768430352
MSV3drs768430352
GWAS Ctlgrs768430352
Max Magnitude0
ClinVar
Risk rs768430352(A;A)
Alt rs768430352(A;A)
Reference rs768430352(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222232G>A; NC_000019.9:g.11222232G>C
CLNSRC LDLR @ LOVD
CLNACC RCV000237712.1, RCV000238166.1,