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rs11678387

From SNPedia

Orientationplus
Stabilizedplus
Make rs11678387(A;A)
Make rs11678387(A;G)
Make rs11678387(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome2
Position120181814
is asnp
is mentioned by
dbSNPrs11678387
dbSNP (old)rs11678387
ClinGenrs11678387
ebirs11678387
HLIrs11678387
Exacrs11678387
Gnomadrs11678387
Varsomers11678387
Maprs11678387
PheGenIrs11678387
Biobankrs11678387
1000 genomesrs11678387
hgdprs11678387
ensemblrs11678387
gopubmedrs11678387
geneviewrs11678387
scholarrs11678387
googlers11678387
pharmgkbrs11678387
gwascentralrs11678387
openSNPrs11678387
23andMers11678387
23andMe allrs11678387
SNPshotrs11678387
SNPdbers11678387
MSV3drs11678387
GWAS Ctlgrs11678387
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 29625478] Genetic Risk Factors for Radiation Vasculopathy.