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rs1064794377

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position32339264
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794377
dbSNP (old)rs1064794377
ClinGenrs1064794377
ebirs1064794377
HLIrs1064794377
Exacrs1064794377
Gnomadrs1064794377
Varsomers1064794377
Maprs1064794377
PheGenIrs1064794377
Biobankrs1064794377
1000 genomesrs1064794377
hgdprs1064794377
ensemblrs1064794377
gopubmedrs1064794377
geneviewrs1064794377
scholarrs1064794377
googlers1064794377
pharmgkbrs1064794377
gwascentralrs1064794377
openSNPrs1064794377
23andMers1064794377
23andMe allrs1064794377
SNPshotrs1064794377
SNPdbers1064794377
MSV3drs1064794377
GWAS Ctlgrs1064794377
Max Magnitude0
ClinVar
Risk rs1064794377(-;-)
Alt rs1064794377(-;-)
Reference Rs1064794377(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32913401delG
CLNSRC
CLNACC RCV000485455.1,