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

rs774723292

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774723292(C;T)
Make rs774723292(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11105249
GeneLDLR
is asnp
is mentioned by
dbSNPrs774723292
ebirs774723292
HLIrs774723292
Exacrs774723292
Varsomers774723292
Maprs774723292
PheGenIrs774723292
hapmaprs774723292
1000 genomesrs774723292
hgdprs774723292
ensemblrs774723292
gopubmedrs774723292
geneviewrs774723292
scholarrs774723292
googlers774723292
pharmgkbrs774723292
gwascentralrs774723292
openSNPrs774723292
23andMers774723292
23andMe allrs774723292
SNP Nexus

SNPshotrs774723292
SNPdbers774723292
MSV3drs774723292
GWAS Ctlgrs774723292
Max Magnitude0
ClinVar
Risk rs774723292(T;T)
Alt rs774723292(T;T)
Reference rs774723292(C;C)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11215925C>T
CLNSRC LDLR @ LOVD
CLNACC RCV000238127.1,