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rs875989916

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs875989916(-;-)
Make rs875989916(-;GTGG)
Make rs875989916(GTGG;GTGG)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11111574
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs875989916
ebirs875989916
HLIrs875989916
Exacrs875989916
Varsomers875989916
Maprs875989916
PheGenIrs875989916
hapmaprs875989916
1000 genomesrs875989916
hgdprs875989916
ensemblrs875989916
gopubmedrs875989916
geneviewrs875989916
scholarrs875989916
googlers875989916
pharmgkbrs875989916
gwascentralrs875989916
openSNPrs875989916
23andMers875989916
23andMe allrs875989916
SNP Nexus

SNPshotrs875989916
SNPdbers875989916
MSV3drs875989916
GWAS Ctlgrs875989916
Max Magnitude0
ClinVar
Risk rs875989916(GGGT;GGGT)
Alt rs875989916(GGGT;GGGT)
Reference rs875989916(;)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222247_11222250dupGTGG
CLNSRC LDLR @ LOVD
CLNACC RCV000211651.2,