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rs1870634

From SNPedia

Orientationminus
Stabilizedminus
Make rs1870634(A;A)
Make rs1870634(A;C)
Make rs1870634(C;C)
ReferenceGRCh38.p7 38.3/151
Chromosome10
Position43985363
is asnp
is mentioned by
dbSNPrs1870634
dbSNP (classic)rs1870634
ClinGenrs1870634
ebirs1870634
HLIrs1870634
Exacrs1870634
Gnomadrs1870634
Varsomers1870634
LitVarrs1870634
Maprs1870634
PheGenIrs1870634
Biobankrs1870634
1000 genomesrs1870634
hgdprs1870634
ensemblrs1870634
geneviewrs1870634
scholarrs1870634
googlers1870634
pharmgkbrs1870634
gwascentralrs1870634
openSNPrs1870634
23andMers1870634
23andMe allrs1870634
SNPshotrs1870634
SNPdbers1870634
MSV3drs1870634
GWAS Ctlgrs1870634
Max Magnitude

[PMID 29654577] Association of the rs1870634 Variant in Long Intergenic Non-protein Coding RNA 841 with Coronary Artery Disease: A GWAS-Replication Study in an Iranian Population.