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rs1060502437

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502437(-;-)
Make rs1060502437(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32336829
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502437
dbSNP (old)rs1060502437
ClinGenrs1060502437
ebirs1060502437
HLIrs1060502437
Exacrs1060502437
Gnomadrs1060502437
Varsomers1060502437
Maprs1060502437
PheGenIrs1060502437
Biobankrs1060502437
1000 genomesrs1060502437
hgdprs1060502437
ensemblrs1060502437
gopubmedrs1060502437
geneviewrs1060502437
scholarrs1060502437
googlers1060502437
pharmgkbrs1060502437
gwascentralrs1060502437
openSNPrs1060502437
23andMers1060502437
23andMe allrs1060502437
SNPshotrs1060502437
SNPdbers1060502437
MSV3drs1060502437
GWAS Ctlgrs1060502437
Max Magnitude0
ClinVar
Risk rs1060502437(-;-)
Alt rs1060502437(-;-)
Reference Rs1060502437(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.32910966delA
CLNSRC
CLNACC RCV000471125.1,