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rs879254907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 5 Familial Hypercholesterolemia
(C;G) 5 Familial Hypercholesterolemia
(G;G) 0 common in clinvar
(G;T) 5 Familial Hypercholesterolemia


Make rs879254907(A;A)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position11113625
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs879254907
dbSNP (classic)rs879254907
ClinGenrs879254907
ebirs879254907
HLIrs879254907
Exacrs879254907
Gnomadrs879254907
Varsomers879254907
LitVarrs879254907
Maprs879254907
PheGenIrs879254907
Biobankrs879254907
1000 genomesrs879254907
hgdprs879254907
ensemblrs879254907
geneviewrs879254907
scholarrs879254907
googlers879254907
pharmgkbrs879254907
gwascentralrs879254907
openSNPrs879254907
23andMers879254907
SNPshotrs879254907
SNPdbers879254907
MSV3drs879254907
GWAS Ctlgrs879254907
Max Magnitude5
ClinVar
Risk rs879254907(A;A) rs879254907(T;T)
Alt rs879254907(A;A) rs879254907(T;T)
Reference Rs879254907(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224301G>A; NC_000019.9:g.11224301G>T
CLNSRC LDLR @ LOVD
CLNACC RCV000238550.1, RCV000237631.1,