Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502400(-;-)
Make rs1060502400(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position32340575
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1060502400
dbSNP (old)rs1060502400
ClinGenrs1060502400
ebirs1060502400
HLIrs1060502400
Exacrs1060502400
Gnomadrs1060502400
Varsomers1060502400
LitVarrs1060502400
Maprs1060502400
PheGenIrs1060502400
Biobankrs1060502400
1000 genomesrs1060502400
hgdprs1060502400
ensemblrs1060502400
gopubmedrs1060502400
geneviewrs1060502400
scholarrs1060502400
googlers1060502400
pharmgkbrs1060502400
gwascentralrs1060502400
openSNPrs1060502400
23andMers1060502400
23andMe allrs1060502400
SNPshotrs1060502400
SNPdbers1060502400
MSV3drs1060502400
GWAS Ctlgrs1060502400
Max Magnitude0
ClinVar
Risk rs1060502400(-;-)
Alt rs1060502400(-;-)
Reference Rs1060502400(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.32914712delC
CLNSRC
CLNACC RCV000463808.1,