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rs1057519673

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 5 Familial Hypercholesterolemia
(C;C) 0 common in clinvar


Make rs1057519673(-;-)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11113705
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1057519673
dbSNP (old)rs1057519673
ClinGenrs1057519673
ebirs1057519673
HLIrs1057519673
Exacrs1057519673
Gnomadrs1057519673
Varsomers1057519673
Maprs1057519673
PheGenIrs1057519673
Biobankrs1057519673
1000 genomesrs1057519673
hgdprs1057519673
ensemblrs1057519673
gopubmedrs1057519673
geneviewrs1057519673
scholarrs1057519673
googlers1057519673
pharmgkbrs1057519673
gwascentralrs1057519673
openSNPrs1057519673
23andMers1057519673
23andMe allrs1057519673
SNPshotrs1057519673
SNPdbers1057519673
MSV3drs1057519673
GWAS Ctlgrs1057519673
Max Magnitude5
ClinVar
Risk rs1057519673(-;-)
Alt rs1057519673(-;-)
Reference Rs1057519673(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224381delC
CLNSRC
CLNACC RCV000417249.1,