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rs1064794852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome13
Position32316421
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794852
dbSNP (old)rs1064794852
ClinGenrs1064794852
ebirs1064794852
HLIrs1064794852
Exacrs1064794852
Gnomadrs1064794852
Varsomers1064794852
Maprs1064794852
PheGenIrs1064794852
Biobankrs1064794852
1000 genomesrs1064794852
hgdprs1064794852
ensemblrs1064794852
gopubmedrs1064794852
geneviewrs1064794852
scholarrs1064794852
googlers1064794852
pharmgkbrs1064794852
gwascentralrs1064794852
openSNPrs1064794852
23andMers1064794852
23andMe allrs1064794852
SNPshotrs1064794852
SNPdbers1064794852
MSV3drs1064794852
GWAS Ctlgrs1064794852
Max Magnitude0
ClinVar
Risk rs1064794852(-;-)
Alt rs1064794852(-;-)
Reference Rs1064794852(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32890558_32890559delGA
CLNSRC
CLNACC RCV000478133.1,