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rs1064794115

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Chromosome13
Position32325108
GeneBRCA2
is asnp
is mentioned by
dbSNPrs1064794115
dbSNP (old)rs1064794115
ClinGenrs1064794115
ebirs1064794115
HLIrs1064794115
Exacrs1064794115
Gnomadrs1064794115
Varsomers1064794115
Maprs1064794115
PheGenIrs1064794115
Biobankrs1064794115
1000 genomesrs1064794115
hgdprs1064794115
ensemblrs1064794115
gopubmedrs1064794115
geneviewrs1064794115
scholarrs1064794115
googlers1064794115
pharmgkbrs1064794115
gwascentralrs1064794115
openSNPrs1064794115
23andMers1064794115
23andMe allrs1064794115
SNPshotrs1064794115
SNPdbers1064794115
MSV3drs1064794115
GWAS Ctlgrs1064794115
Max Magnitude0
ClinVar
Risk rs1064794115(-;-)
Alt rs1064794115(-;-)
Reference Rs1064794115(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32899245_32899246delCT
CLNSRC
CLNACC RCV000479498.1,