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rs1064795789

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome13
Position32339948
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064795789
dbSNP (old)rs1064795789
ClinGenrs1064795789
ebirs1064795789
HLIrs1064795789
Exacrs1064795789
Gnomadrs1064795789
Varsomers1064795789
Maprs1064795789
PheGenIrs1064795789
Biobankrs1064795789
1000 genomesrs1064795789
hgdprs1064795789
ensemblrs1064795789
gopubmedrs1064795789
geneviewrs1064795789
scholarrs1064795789
googlers1064795789
pharmgkbrs1064795789
gwascentralrs1064795789
openSNPrs1064795789
23andMers1064795789
23andMe allrs1064795789
SNPshotrs1064795789
SNPdbers1064795789
MSV3drs1064795789
GWAS Ctlgrs1064795789
Max Magnitude0
ClinVar
Risk rs1064795789(-;-)
Alt rs1064795789(-;-)
Reference Rs1064795789(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32914085delA
CLNSRC
CLNACC RCV000482637.1,