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rs1064795578

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome13
Position32363201
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064795578
dbSNP (old)rs1064795578
ClinGenrs1064795578
ebirs1064795578
HLIrs1064795578
Exacrs1064795578
Gnomadrs1064795578
Varsomers1064795578
Maprs1064795578
PheGenIrs1064795578
Biobankrs1064795578
1000 genomesrs1064795578
hgdprs1064795578
ensemblrs1064795578
gopubmedrs1064795578
geneviewrs1064795578
scholarrs1064795578
googlers1064795578
pharmgkbrs1064795578
gwascentralrs1064795578
openSNPrs1064795578
23andMers1064795578
23andMe allrs1064795578
SNPshotrs1064795578
SNPdbers1064795578
MSV3drs1064795578
GWAS Ctlgrs1064795578
Max Magnitude0
ClinVar
Risk rs1064795578(-;-)
Alt rs1064795578(-;-)
Reference Rs1064795578(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32937338delA
CLNSRC
CLNACC RCV000486140.1,