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rs773658037

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773658037(A;A)
Make rs773658037(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113338
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs773658037
ebirs773658037
HLIrs773658037
Exacrs773658037
Varsomers773658037
Maprs773658037
PheGenIrs773658037
hapmaprs773658037
1000 genomesrs773658037
hgdprs773658037
ensemblrs773658037
gopubmedrs773658037
geneviewrs773658037
scholarrs773658037
googlers773658037
pharmgkbrs773658037
gwascentralrs773658037
openSNPrs773658037
23andMers773658037
23andMe allrs773658037
SNP Nexus

SNPshotrs773658037
SNPdbers773658037
MSV3drs773658037
GWAS Ctlgrs773658037
Max Magnitude0
ClinVar
Risk rs773658037(A;A)
Alt rs773658037(A;A)
Reference rs773658037(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224014G>A; NC_000019.9:g.11224014G>C; NC_000019.9:g.11224014G>T
CLNSRC LDLR @ LOVD
CLNACC RCV000237115.1, RCV000238315.1, RCV000237152.1,