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rs1064796073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome13
Position32333311
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064796073
dbSNP (old)rs1064796073
ClinGenrs1064796073
ebirs1064796073
HLIrs1064796073
Exacrs1064796073
Gnomadrs1064796073
Varsomers1064796073
Maprs1064796073
PheGenIrs1064796073
Biobankrs1064796073
1000 genomesrs1064796073
hgdprs1064796073
ensemblrs1064796073
gopubmedrs1064796073
geneviewrs1064796073
scholarrs1064796073
googlers1064796073
pharmgkbrs1064796073
gwascentralrs1064796073
openSNPrs1064796073
23andMers1064796073
23andMe allrs1064796073
SNPshotrs1064796073
SNPdbers1064796073
MSV3drs1064796073
GWAS Ctlgrs1064796073
Max Magnitude0
ClinVar
Risk rs1064796073(-;-)
Alt rs1064796073(-;-)
Reference Rs1064796073(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32907448delA
CLNSRC
CLNACC RCV000480264.1,