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rs1064793873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome18
Position47869288
GeneSMAD2
is asnp
is mentioned by
dbSNPrs1064793873
dbSNP (old)rs1064793873
ClinGenrs1064793873
ebirs1064793873
HLIrs1064793873
Exacrs1064793873
Gnomadrs1064793873
Varsomers1064793873
Maprs1064793873
PheGenIrs1064793873
Biobankrs1064793873
1000 genomesrs1064793873
hgdprs1064793873
ensemblrs1064793873
gopubmedrs1064793873
geneviewrs1064793873
scholarrs1064793873
googlers1064793873
pharmgkbrs1064793873
gwascentralrs1064793873
openSNPrs1064793873
23andMers1064793873
23andMe allrs1064793873
SNPshotrs1064793873
SNPdbers1064793873
MSV3drs1064793873
GWAS Ctlgrs1064793873
Max Magnitude0
ClinVar
Risk rs1064793873(T;T)
Alt rs1064793873(T;T)
Reference Rs1064793873(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.45395659C>A
CLNSRC
CLNACC RCV000480930.1,