Have questions? Visit https://www.reddit.com/r/SNPedia

rs875989908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs875989908(-;GGGACTGGTCAGATGAACC)
Make rs875989908(GGGACTGGTCAGATGAACC;GGGACTGGTCAGATGAACC)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11107500
GeneLDLR
is asnp
is mentioned by
dbSNPrs875989908
dbSNP (old)rs875989908
ClinGenrs875989908
ebirs875989908
HLIrs875989908
Exacrs875989908
Gnomadrs875989908
Varsomers875989908
Maprs875989908
PheGenIrs875989908
Biobankrs875989908
1000 genomesrs875989908
hgdprs875989908
ensemblrs875989908
gopubmedrs875989908
geneviewrs875989908
scholarrs875989908
googlers875989908
pharmgkbrs875989908
gwascentralrs875989908
openSNPrs875989908
23andMers875989908
23andMe allrs875989908
SNP Nexus

SNPshotrs875989908
SNPdbers875989908
MSV3drs875989908
GWAS Ctlgrs875989908
Max Magnitude0
ClinVar
Risk rs875989908(CCGGGACTGGTCAGATGAA;CCGGGACTGGTCAGATGAA)
Alt rs875989908(CCGGGACTGGTCAGATGAA;CCGGGACTGGTCAGATGAA)
Reference Rs875989908(-;-)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11218158_11218176dup19
CLNSRC
CLNACC RCV000211587.1,