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rs730880284

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880284(A;A)
Make rs730880284(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position169612928
GeneSELP
is asnp
is mentioned by
dbSNPrs730880284
ebirs730880284
HLIrs730880284
Exacrs730880284
Varsomers730880284
Maprs730880284
PheGenIrs730880284
hapmaprs730880284
1000 genomesrs730880284
hgdprs730880284
ensemblrs730880284
gopubmedrs730880284
geneviewrs730880284
scholarrs730880284
googlers730880284
pharmgkbrs730880284
gwascentralrs730880284
openSNPrs730880284
23andMers730880284
23andMe allrs730880284
SNP Nexus

SNPshotrs730880284
SNPdbers730880284
MSV3drs730880284
GWAS Ctlgrs730880284
Max Magnitude0
ClinVar
Risk rs730880284(A,C;A,C)
Alt rs730880284(A,C;A,C)
Reference rs730880284(G;G)
Significance Probable-Pathogenic
Disease Premature coronary artery disease
Variation info
Gene SELP
CLNDBN Premature coronary artery disease
Reversed 1
HGVS NC_000001.10:g.169582166C>T
CLNSRC
CLNACC RCV000157648.1,