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rs764797225

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764797225(-;-)
Make rs764797225(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11102776
GeneLDLR
is asnp
is mentioned by
dbSNPrs764797225
ebirs764797225
HLIrs764797225
Exacrs764797225
Varsomers764797225
Maprs764797225
PheGenIrs764797225
hapmaprs764797225
1000 genomesrs764797225
hgdprs764797225
ensemblrs764797225
gopubmedrs764797225
geneviewrs764797225
scholarrs764797225
googlers764797225
pharmgkbrs764797225
gwascentralrs764797225
openSNPrs764797225
23andMers764797225
23andMe allrs764797225
SNP Nexus

SNPshotrs764797225
SNPdbers764797225
MSV3drs764797225
GWAS Ctlgrs764797225
Max Magnitude0
ClinVar
Risk rs764797225(;)
Alt rs764797225(;)
Reference rs764797225(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11213452delG
CLNSRC LDLR @ LOVD
CLNACC RCV000237566.1,