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

rs1060502459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060502459(A;A)
Make rs1060502459(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32362593
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502459
dbSNP (old)rs1060502459
ClinGenrs1060502459
ebirs1060502459
HLIrs1060502459
Exacrs1060502459
Gnomadrs1060502459
Varsomers1060502459
Maprs1060502459
PheGenIrs1060502459
Biobankrs1060502459
1000 genomesrs1060502459
hgdprs1060502459
ensemblrs1060502459
gopubmedrs1060502459
geneviewrs1060502459
scholarrs1060502459
googlers1060502459
pharmgkbrs1060502459
gwascentralrs1060502459
openSNPrs1060502459
23andMers1060502459
23andMe allrs1060502459
SNPshotrs1060502459
SNPdbers1060502459
MSV3drs1060502459
GWAS Ctlgrs1060502459
Max Magnitude0
ClinVar
Risk rs1060502459(A;A)
Alt rs1060502459(A;A)
Reference Rs1060502459(T;T)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome not provided
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32936730T>A; NC_000013.10:g.32936730T>C
CLNSRC
CLNACC RCV000465347.1, RCV000493105.1,