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rs1064794647

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position32340618
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794647
dbSNP (old)rs1064794647
ClinGenrs1064794647
ebirs1064794647
HLIrs1064794647
Exacrs1064794647
Gnomadrs1064794647
Varsomers1064794647
Maprs1064794647
PheGenIrs1064794647
Biobankrs1064794647
1000 genomesrs1064794647
hgdprs1064794647
ensemblrs1064794647
gopubmedrs1064794647
geneviewrs1064794647
scholarrs1064794647
googlers1064794647
pharmgkbrs1064794647
gwascentralrs1064794647
openSNPrs1064794647
23andMers1064794647
23andMe allrs1064794647
SNPshotrs1064794647
SNPdbers1064794647
MSV3drs1064794647
GWAS Ctlgrs1064794647
Max Magnitude0
ClinVar
Risk rs1064794647(-;-)
Alt rs1064794647(-;-)
Reference Rs1064794647(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32914755delC
CLNSRC
CLNACC RCV000478351.1,