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rs1064796790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome10
Position110602825
GeneSMC3
is asnp
is mentioned by
dbSNPrs1064796790
dbSNP (old)rs1064796790
ClinGenrs1064796790
ebirs1064796790
HLIrs1064796790
Exacrs1064796790
Gnomadrs1064796790
Varsomers1064796790
Maprs1064796790
PheGenIrs1064796790
Biobankrs1064796790
1000 genomesrs1064796790
hgdprs1064796790
ensemblrs1064796790
gopubmedrs1064796790
geneviewrs1064796790
scholarrs1064796790
googlers1064796790
pharmgkbrs1064796790
gwascentralrs1064796790
openSNPrs1064796790
23andMers1064796790
23andMe allrs1064796790
SNPshotrs1064796790
SNPdbers1064796790
MSV3drs1064796790
GWAS Ctlgrs1064796790
Max Magnitude0
ClinVar
Risk rs1064796790(T;T)
Alt rs1064796790(T;T)
Reference Rs1064796790(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMC3
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112362583G>T
CLNSRC
CLNACC RCV000484780.1,