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rs2104543

From SNPedia

Orientationplus
Stabilizedplus
Make rs2104543(C;C)
Make rs2104543(C;T)
Make rs2104543(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position94670214
is asnp
is mentioned by
dbSNPrs2104543
dbSNP (old)rs2104543
ClinGenrs2104543
ebirs2104543
HLIrs2104543
Exacrs2104543
Gnomadrs2104543
Varsomers2104543
Maprs2104543
PheGenIrs2104543
Biobankrs2104543
1000 genomesrs2104543
hgdprs2104543
ensemblrs2104543
gopubmedrs2104543
geneviewrs2104543
scholarrs2104543
googlers2104543
pharmgkbrs2104543
gwascentralrs2104543
openSNPrs2104543
23andMers2104543
23andMe allrs2104543
SNPshotrs2104543
SNPdbers2104543
MSV3drs2104543
GWAS Ctlgrs2104543
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 28280103] Association of genetic variant and platelet function in patients undergoing neuroendovascular stenting.