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rs1064793471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome13
Position32340835
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064793471
dbSNP (old)rs1064793471
ClinGenrs1064793471
ebirs1064793471
HLIrs1064793471
Exacrs1064793471
Gnomadrs1064793471
Varsomers1064793471
Maprs1064793471
PheGenIrs1064793471
Biobankrs1064793471
1000 genomesrs1064793471
hgdprs1064793471
ensemblrs1064793471
gopubmedrs1064793471
geneviewrs1064793471
scholarrs1064793471
googlers1064793471
pharmgkbrs1064793471
gwascentralrs1064793471
openSNPrs1064793471
23andMers1064793471
23andMe allrs1064793471
SNPshotrs1064793471
SNPdbers1064793471
MSV3drs1064793471
GWAS Ctlgrs1064793471
Max Magnitude0
ClinVar
Risk rs1064793471(-;-)
Alt rs1064793471(-;-)
Reference Rs1064793471(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32914972delA
CLNSRC
CLNACC RCV000487195.1,