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rs1064793467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome13
Position32336691
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064793467
dbSNP (old)rs1064793467
ClinGenrs1064793467
ebirs1064793467
HLIrs1064793467
Exacrs1064793467
Gnomadrs1064793467
Varsomers1064793467
Maprs1064793467
PheGenIrs1064793467
Biobankrs1064793467
1000 genomesrs1064793467
hgdprs1064793467
ensemblrs1064793467
gopubmedrs1064793467
geneviewrs1064793467
scholarrs1064793467
googlers1064793467
pharmgkbrs1064793467
gwascentralrs1064793467
openSNPrs1064793467
23andMers1064793467
23andMe allrs1064793467
SNPshotrs1064793467
SNPdbers1064793467
MSV3drs1064793467
GWAS Ctlgrs1064793467
Max Magnitude0
ClinVar
Risk rs1064793467(-;-)
Alt rs1064793467(-;-)
Reference Rs1064793467(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32910828delT
CLNSRC
CLNACC RCV000480214.1,