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rs1064794550

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position32337387
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794550
dbSNP (old)rs1064794550
ClinGenrs1064794550
ebirs1064794550
HLIrs1064794550
Exacrs1064794550
Gnomadrs1064794550
Varsomers1064794550
LitVarrs1064794550
Maprs1064794550
PheGenIrs1064794550
Biobankrs1064794550
1000 genomesrs1064794550
hgdprs1064794550
ensemblrs1064794550
gopubmedrs1064794550
geneviewrs1064794550
scholarrs1064794550
googlers1064794550
pharmgkbrs1064794550
gwascentralrs1064794550
openSNPrs1064794550
23andMers1064794550
23andMe allrs1064794550
SNPshotrs1064794550
SNPdbers1064794550
MSV3drs1064794550
GWAS Ctlgrs1064794550
Max Magnitude0
ClinVar
Risk rs1064794550(-;-)
Alt rs1064794550(-;-)
Reference Rs1064794550(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32911524delC
CLNSRC
CLNACC RCV000483366.1,