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rs1064795431

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position93104044
GeneSAMD9
is asnp
is mentioned by
dbSNPrs1064795431
dbSNP (old)rs1064795431
ClinGenrs1064795431
ebirs1064795431
HLIrs1064795431
Exacrs1064795431
Gnomadrs1064795431
Varsomers1064795431
Maprs1064795431
PheGenIrs1064795431
Biobankrs1064795431
1000 genomesrs1064795431
hgdprs1064795431
ensemblrs1064795431
gopubmedrs1064795431
geneviewrs1064795431
scholarrs1064795431
googlers1064795431
pharmgkbrs1064795431
gwascentralrs1064795431
openSNPrs1064795431
23andMers1064795431
23andMe allrs1064795431
SNPshotrs1064795431
SNPdbers1064795431
MSV3drs1064795431
GWAS Ctlgrs1064795431
Max Magnitude0
ClinVar
Risk rs1064795431(A;A)
Alt rs1064795431(A;A)
Reference Rs1064795431(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SAMD9
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.92733357C>T
CLNSRC
CLNACC RCV000479048.1,