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rs1064794059

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position32319171
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794059
dbSNP (old)rs1064794059
ClinGenrs1064794059
ebirs1064794059
HLIrs1064794059
Exacrs1064794059
Gnomadrs1064794059
Varsomers1064794059
Maprs1064794059
PheGenIrs1064794059
Biobankrs1064794059
1000 genomesrs1064794059
hgdprs1064794059
ensemblrs1064794059
gopubmedrs1064794059
geneviewrs1064794059
scholarrs1064794059
googlers1064794059
pharmgkbrs1064794059
gwascentralrs1064794059
openSNPrs1064794059
23andMers1064794059
23andMe allrs1064794059
SNPshotrs1064794059
SNPdbers1064794059
MSV3drs1064794059
GWAS Ctlgrs1064794059
Max Magnitude0
ClinVar
Risk rs1064794059(-;-)
Alt rs1064794059(-;-)
Reference Rs1064794059(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32893308delC
CLNSRC
CLNACC RCV000479560.1,