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rs1060502482

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502482(-;-)
Make rs1060502482(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32356439
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502482
dbSNP (old)rs1060502482
ClinGenrs1060502482
ebirs1060502482
HLIrs1060502482
Exacrs1060502482
Gnomadrs1060502482
Varsomers1060502482
Maprs1060502482
PheGenIrs1060502482
Biobankrs1060502482
1000 genomesrs1060502482
hgdprs1060502482
ensemblrs1060502482
gopubmedrs1060502482
geneviewrs1060502482
scholarrs1060502482
googlers1060502482
pharmgkbrs1060502482
gwascentralrs1060502482
openSNPrs1060502482
23andMers1060502482
23andMe allrs1060502482
SNPshotrs1060502482
SNPdbers1060502482
MSV3drs1060502482
GWAS Ctlgrs1060502482
Max Magnitude0
ClinVar
Risk rs1060502482(-;-)
Alt rs1060502482(-;-)
Reference Rs1060502482(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.32930576delA
CLNSRC
CLNACC RCV000461479.1,