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rs1064795072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position32316475
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064795072
dbSNP (old)rs1064795072
ClinGenrs1064795072
ebirs1064795072
HLIrs1064795072
Exacrs1064795072
Gnomadrs1064795072
Varsomers1064795072
Maprs1064795072
PheGenIrs1064795072
Biobankrs1064795072
1000 genomesrs1064795072
hgdprs1064795072
ensemblrs1064795072
gopubmedrs1064795072
geneviewrs1064795072
scholarrs1064795072
googlers1064795072
pharmgkbrs1064795072
gwascentralrs1064795072
openSNPrs1064795072
23andMers1064795072
23andMe allrs1064795072
SNPshotrs1064795072
SNPdbers1064795072
MSV3drs1064795072
GWAS Ctlgrs1064795072
Max Magnitude0
ClinVar
Risk rs1064795072(-;-)
Alt rs1064795072(-;-)
Reference Rs1064795072(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32890612delC
CLNSRC
CLNACC RCV000478121.1,