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rs765696008

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765696008(A;A)
Make rs765696008(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113268
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs765696008
ebirs765696008
HLIrs765696008
Exacrs765696008
Varsomers765696008
Maprs765696008
PheGenIrs765696008
hapmaprs765696008
1000 genomesrs765696008
hgdprs765696008
ensemblrs765696008
gopubmedrs765696008
geneviewrs765696008
scholarrs765696008
googlers765696008
pharmgkbrs765696008
gwascentralrs765696008
openSNPrs765696008
23andMers765696008
23andMe allrs765696008
SNP Nexus

SNPshotrs765696008
SNPdbers765696008
MSV3drs765696008
GWAS Ctlgrs765696008
Max Magnitude0
ClinVar
Risk rs765696008(A;A)
Alt rs765696008(A;A)
Reference rs765696008(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11223944G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000211627.2,