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rs1064794921

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome13
Position32338236
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794921
dbSNP (old)rs1064794921
ClinGenrs1064794921
ebirs1064794921
HLIrs1064794921
Exacrs1064794921
Gnomadrs1064794921
Varsomers1064794921
Maprs1064794921
PheGenIrs1064794921
Biobankrs1064794921
1000 genomesrs1064794921
hgdprs1064794921
ensemblrs1064794921
gopubmedrs1064794921
geneviewrs1064794921
scholarrs1064794921
googlers1064794921
pharmgkbrs1064794921
gwascentralrs1064794921
openSNPrs1064794921
23andMers1064794921
23andMe allrs1064794921
SNPshotrs1064794921
SNPdbers1064794921
MSV3drs1064794921
GWAS Ctlgrs1064794921
Max Magnitude0
ClinVar
Risk rs1064794921(-;-)
Alt rs1064794921(-;-)
Reference Rs1064794921(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32912373delT
CLNSRC
CLNACC RCV000486768.1,