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rs1064794708

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome13
Position32339032
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794708
dbSNP (old)rs1064794708
ClinGenrs1064794708
ebirs1064794708
HLIrs1064794708
Exacrs1064794708
Gnomadrs1064794708
Varsomers1064794708
Maprs1064794708
PheGenIrs1064794708
Biobankrs1064794708
1000 genomesrs1064794708
hgdprs1064794708
ensemblrs1064794708
gopubmedrs1064794708
geneviewrs1064794708
scholarrs1064794708
googlers1064794708
pharmgkbrs1064794708
gwascentralrs1064794708
openSNPrs1064794708
23andMers1064794708
23andMe allrs1064794708
SNPshotrs1064794708
SNPdbers1064794708
MSV3drs1064794708
GWAS Ctlgrs1064794708
Max Magnitude0
ClinVar
Risk rs1064794708(-;-)
Alt rs1064794708(-;-)
Reference Rs1064794708(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32913169delT
CLNSRC
CLNACC RCV000482054.1,