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rs1060502392

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502392(-;-)
Make rs1060502392(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32340929
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502392
dbSNP (old)rs1060502392
ClinGenrs1060502392
ebirs1060502392
HLIrs1060502392
Exacrs1060502392
Gnomadrs1060502392
Varsomers1060502392
Maprs1060502392
PheGenIrs1060502392
Biobankrs1060502392
1000 genomesrs1060502392
hgdprs1060502392
ensemblrs1060502392
gopubmedrs1060502392
geneviewrs1060502392
scholarrs1060502392
googlers1060502392
pharmgkbrs1060502392
gwascentralrs1060502392
openSNPrs1060502392
23andMers1060502392
23andMe allrs1060502392
SNPshotrs1060502392
SNPdbers1060502392
MSV3drs1060502392
GWAS Ctlgrs1060502392
Max Magnitude0
ClinVar
Risk rs1060502392(-;-)
Alt rs1060502392(-;-)
Reference Rs1060502392(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.32915066delA
CLNSRC
CLNACC RCV000475177.1,