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rs1064792962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAAGCA;CAAGCA) 0 common in clinvar
Chromosome13
Position32354968
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064792962
dbSNP (old)rs1064792962
ClinGenrs1064792962
ebirs1064792962
HLIrs1064792962
Exacrs1064792962
Gnomadrs1064792962
Varsomers1064792962
LitVarrs1064792962
Maprs1064792962
PheGenIrs1064792962
Biobankrs1064792962
1000 genomesrs1064792962
hgdprs1064792962
ensemblrs1064792962
gopubmedrs1064792962
geneviewrs1064792962
scholarrs1064792962
googlers1064792962
pharmgkbrs1064792962
gwascentralrs1064792962
openSNPrs1064792962
23andMers1064792962
23andMe allrs1064792962
SNPshotrs1064792962
SNPdbers1064792962
MSV3drs1064792962
GWAS Ctlgrs1064792962
Max Magnitude0
ClinVar
Risk rs1064792962(GC;GC)
Alt rs1064792962(GC;GC)
Reference Rs1064792962(CAAGCA;CAAGCA)
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.32929105_32929110delCAAGCAinsGC
CLNSRC
CLNACC RCV000465804.1,