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rs876657697

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657697(-;-)
Make rs876657697(-;C)
Make rs876657697(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113604
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs876657697
ebirs876657697
HLIrs876657697
Exacrs876657697
Varsomers876657697
Maprs876657697
PheGenIrs876657697
hapmaprs876657697
1000 genomesrs876657697
hgdprs876657697
ensemblrs876657697
gopubmedrs876657697
geneviewrs876657697
scholarrs876657697
googlers876657697
pharmgkbrs876657697
gwascentralrs876657697
openSNPrs876657697
23andMers876657697
23andMe allrs876657697
SNP Nexus

SNPshotrs876657697
SNPdbers876657697
MSV3drs876657697
GWAS Ctlgrs876657697
Max Magnitude0
ClinVar
Risk rs876657697(C;C)
Alt rs876657697(C;C)
Reference rs876657697(;)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224280dupC
CLNSRC LDLR @ LOVD
CLNACC RCV000216563.2,