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rs1060502403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502403(-;-)
Make rs1060502403(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32332670
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502403
dbSNP (old)rs1060502403
ClinGenrs1060502403
ebirs1060502403
HLIrs1060502403
Exacrs1060502403
Gnomadrs1060502403
Varsomers1060502403
LitVarrs1060502403
Maprs1060502403
PheGenIrs1060502403
Biobankrs1060502403
1000 genomesrs1060502403
hgdprs1060502403
ensemblrs1060502403
gopubmedrs1060502403
geneviewrs1060502403
scholarrs1060502403
googlers1060502403
pharmgkbrs1060502403
gwascentralrs1060502403
openSNPrs1060502403
23andMers1060502403
23andMe allrs1060502403
SNPshotrs1060502403
SNPdbers1060502403
MSV3drs1060502403
GWAS Ctlgrs1060502403
Max Magnitude0
ClinVar
Risk rs1060502403(-;-)
Alt rs1060502403(-;-)
Reference Rs1060502403(C;C)
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.32906807delC
CLNSRC
CLNACC RCV000474731.1,