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rs1064793785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome13
Position32338494
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064793785
dbSNP (old)rs1064793785
ClinGenrs1064793785
ebirs1064793785
HLIrs1064793785
Exacrs1064793785
Gnomadrs1064793785
Varsomers1064793785
Maprs1064793785
PheGenIrs1064793785
Biobankrs1064793785
1000 genomesrs1064793785
hgdprs1064793785
ensemblrs1064793785
gopubmedrs1064793785
geneviewrs1064793785
scholarrs1064793785
googlers1064793785
pharmgkbrs1064793785
gwascentralrs1064793785
openSNPrs1064793785
23andMers1064793785
23andMe allrs1064793785
SNPshotrs1064793785
SNPdbers1064793785
MSV3drs1064793785
GWAS Ctlgrs1064793785
Max Magnitude0
ClinVar
Risk rs1064793785(TT;TT)
Alt rs1064793785(TT;TT)
Reference Rs1064793785(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32912631_32912632dupTT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044359.2, RCV000113279.2, RCV000130775.2, RCV000483206.2,