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rs1064793278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position218436147
GeneTGFB2
is asnp
is mentioned by
dbSNPrs1064793278
dbSNP (old)rs1064793278
ClinGenrs1064793278
ebirs1064793278
HLIrs1064793278
Exacrs1064793278
Gnomadrs1064793278
Varsomers1064793278
Maprs1064793278
PheGenIrs1064793278
Biobankrs1064793278
1000 genomesrs1064793278
hgdprs1064793278
ensemblrs1064793278
gopubmedrs1064793278
geneviewrs1064793278
scholarrs1064793278
googlers1064793278
pharmgkbrs1064793278
gwascentralrs1064793278
openSNPrs1064793278
23andMers1064793278
23andMe allrs1064793278
SNPshotrs1064793278
SNPdbers1064793278
MSV3drs1064793278
GWAS Ctlgrs1064793278
Max Magnitude0
ClinVar
Risk rs1064793278(A;A)
Alt rs1064793278(A;A)
Reference Rs1064793278(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218609489G>A
CLNSRC
CLNACC RCV000479243.1,