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rs770744861

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770744861(A;A)
Make rs770744861(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11120405
GeneLDLR
is asnp
is mentioned by
dbSNPrs770744861
ebirs770744861
HLIrs770744861
Exacrs770744861
Varsomers770744861
Maprs770744861
PheGenIrs770744861
hapmaprs770744861
1000 genomesrs770744861
hgdprs770744861
ensemblrs770744861
gopubmedrs770744861
geneviewrs770744861
scholarrs770744861
googlers770744861
pharmgkbrs770744861
gwascentralrs770744861
openSNPrs770744861
23andMers770744861
23andMe allrs770744861
SNP Nexus

SNPshotrs770744861
SNPdbers770744861
MSV3drs770744861
GWAS Ctlgrs770744861
Max Magnitude0
ClinVar
Risk rs770744861(A;A)
Alt rs770744861(A;A)
Reference rs770744861(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11231081G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000238136.1,