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rs13306515

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs13306515(C;T)
Make rs13306515(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11110767
GeneLDLR
is asnp
is mentioned by
dbSNPrs13306515
ebirs13306515
HLIrs13306515
Exacrs13306515
Varsomers13306515
Maprs13306515
PheGenIrs13306515
hapmaprs13306515
1000 genomesrs13306515
hgdprs13306515
ensemblrs13306515
gopubmedrs13306515
geneviewrs13306515
scholarrs13306515
googlers13306515
pharmgkbrs13306515
gwascentralrs13306515
openSNPrs13306515
23andMers13306515
23andMe allrs13306515
SNP Nexus

SNPshotrs13306515
SNPdbers13306515
MSV3drs13306515
GWAS Ctlgrs13306515
Max Magnitude0
ClinVar
Risk rs13306515(T;T)
Alt rs13306515(T;T)
Reference rs13306515(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11221443C>A; NC_000019.9:g.11221443C>G
CLNSRC LDLR @ LOVD
CLNACC RCV000238410.1, RCV000237561.1,