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rs1060502475

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502475(-;-)
Make rs1060502475(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32337432
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502475
dbSNP (old)rs1060502475
ClinGenrs1060502475
ebirs1060502475
HLIrs1060502475
Exacrs1060502475
Gnomadrs1060502475
Varsomers1060502475
Maprs1060502475
PheGenIrs1060502475
Biobankrs1060502475
1000 genomesrs1060502475
hgdprs1060502475
ensemblrs1060502475
gopubmedrs1060502475
geneviewrs1060502475
scholarrs1060502475
googlers1060502475
pharmgkbrs1060502475
gwascentralrs1060502475
openSNPrs1060502475
23andMers1060502475
23andMe allrs1060502475
SNPshotrs1060502475
SNPdbers1060502475
MSV3drs1060502475
GWAS Ctlgrs1060502475
Max Magnitude0
ClinVar
Risk rs1060502475(-;-)
Alt rs1060502475(-;-)
Reference Rs1060502475(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.32911569delA
CLNSRC
CLNACC RCV000468393.1,