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rs146200173

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146200173(C;G)
Make rs146200173(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position11113292
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs146200173
ebirs146200173
HLIrs146200173
Exacrs146200173
Varsomers146200173
Maprs146200173
PheGenIrs146200173
hapmaprs146200173
1000 genomesrs146200173
hgdprs146200173
ensemblrs146200173
gopubmedrs146200173
geneviewrs146200173
scholarrs146200173
googlers146200173
pharmgkbrs146200173
gwascentralrs146200173
openSNPrs146200173
23andMers146200173
23andMe allrs146200173
SNP Nexus

SNPshotrs146200173
SNPdbers146200173
MSV3drs146200173
GWAS Ctlgrs146200173
Max Magnitude0
ClinVar
Risk rs146200173(G;G)
Alt rs146200173(G;G)
Reference rs146200173(C;C)
Significance Probable-Pathogenic
Disease Hypercholesterolaemia Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Hypercholesterolaemia Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11223968C>G
CLNSRC LDLR @ LOVD
CLNACC RCV000148572.1, RCV000238417.1,