Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060502391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502391(-;-)
Make rs1060502391(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32337331
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502391
dbSNP (old)rs1060502391
ClinGenrs1060502391
ebirs1060502391
HLIrs1060502391
Exacrs1060502391
Gnomadrs1060502391
Varsomers1060502391
Maprs1060502391
PheGenIrs1060502391
Biobankrs1060502391
1000 genomesrs1060502391
hgdprs1060502391
ensemblrs1060502391
gopubmedrs1060502391
geneviewrs1060502391
scholarrs1060502391
googlers1060502391
pharmgkbrs1060502391
gwascentralrs1060502391
openSNPrs1060502391
23andMers1060502391
23andMe allrs1060502391
SNPshotrs1060502391
SNPdbers1060502391
MSV3drs1060502391
GWAS Ctlgrs1060502391
Max Magnitude0
ClinVar
Risk rs1060502391(-;-)
Alt rs1060502391(-;-)
Reference Rs1060502391(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32911468delA
CLNSRC
CLNACC RCV000475958.1,