Have questions? Visit https://www.reddit.com/r/SNPedia

rs773064328

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs773064328(C;C)
Make rs773064328(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11111582
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs773064328
ebirs773064328
HLIrs773064328
Exacrs773064328
Varsomers773064328
Maprs773064328
PheGenIrs773064328
hapmaprs773064328
1000 genomesrs773064328
hgdprs773064328
ensemblrs773064328
gopubmedrs773064328
geneviewrs773064328
scholarrs773064328
googlers773064328
pharmgkbrs773064328
gwascentralrs773064328
openSNPrs773064328
23andMers773064328
23andMe allrs773064328
SNP Nexus

SNPshotrs773064328
SNPdbers773064328
MSV3drs773064328
GWAS Ctlgrs773064328
Max Magnitude0
ClinVar
Risk rs773064328(C;C)
Alt rs773064328(C;C)
Reference rs773064328(T;T)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222258T>G
CLNSRC LDLR @ LOVD
CLNACC RCV000238460.1,