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rs1064794337

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position32338774
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794337
dbSNP (old)rs1064794337
ClinGenrs1064794337
ebirs1064794337
HLIrs1064794337
Exacrs1064794337
Gnomadrs1064794337
Varsomers1064794337
Maprs1064794337
PheGenIrs1064794337
Biobankrs1064794337
1000 genomesrs1064794337
hgdprs1064794337
ensemblrs1064794337
gopubmedrs1064794337
geneviewrs1064794337
scholarrs1064794337
googlers1064794337
pharmgkbrs1064794337
gwascentralrs1064794337
openSNPrs1064794337
23andMers1064794337
23andMe allrs1064794337
SNPshotrs1064794337
SNPdbers1064794337
MSV3drs1064794337
GWAS Ctlgrs1064794337
Max Magnitude0
ClinVar
Risk rs1064794337(-;-)
Alt rs1064794337(-;-)
Reference Rs1064794337(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32912911delC
CLNSRC
CLNACC RCV000484635.1,