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rs1060502426

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502426(-;-)
Make rs1060502426(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32338628
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502426
dbSNP (old)rs1060502426
ClinGenrs1060502426
ebirs1060502426
HLIrs1060502426
Exacrs1060502426
Gnomadrs1060502426
Varsomers1060502426
Maprs1060502426
PheGenIrs1060502426
Biobankrs1060502426
1000 genomesrs1060502426
hgdprs1060502426
ensemblrs1060502426
gopubmedrs1060502426
geneviewrs1060502426
scholarrs1060502426
googlers1060502426
pharmgkbrs1060502426
gwascentralrs1060502426
openSNPrs1060502426
23andMers1060502426
23andMe allrs1060502426
SNPshotrs1060502426
SNPdbers1060502426
MSV3drs1060502426
GWAS Ctlgrs1060502426
Max Magnitude0
ClinVar
Risk rs1060502426(-;-)
Alt rs1060502426(-;-)
Reference Rs1060502426(G;G)
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.32912765delG
CLNSRC
CLNACC RCV000471947.1,