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rs1064795851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position32394757
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064795851
dbSNP (old)rs1064795851
ClinGenrs1064795851
ebirs1064795851
HLIrs1064795851
Exacrs1064795851
Gnomadrs1064795851
Varsomers1064795851
Maprs1064795851
PheGenIrs1064795851
Biobankrs1064795851
1000 genomesrs1064795851
hgdprs1064795851
ensemblrs1064795851
gopubmedrs1064795851
geneviewrs1064795851
scholarrs1064795851
googlers1064795851
pharmgkbrs1064795851
gwascentralrs1064795851
openSNPrs1064795851
23andMers1064795851
23andMe allrs1064795851
SNPshotrs1064795851
SNPdbers1064795851
MSV3drs1064795851
GWAS Ctlgrs1064795851
Max Magnitude0
ClinVar
Risk rs1064795851(-;-)
Alt rs1064795851(-;-)
Reference Rs1064795851(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32968894delC
CLNSRC
CLNACC RCV000485937.1,