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rs879255329

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879255329(-;-)
Make rs879255329(-;TT)
Make rs879255329(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339734
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255329
ebirs879255329
HLIrs879255329
Exacrs879255329
Varsomers879255329
Maprs879255329
PheGenIrs879255329
hapmaprs879255329
1000 genomesrs879255329
hgdprs879255329
ensemblrs879255329
gopubmedrs879255329
geneviewrs879255329
scholarrs879255329
googlers879255329
pharmgkbrs879255329
gwascentralrs879255329
openSNPrs879255329
23andMers879255329
23andMe allrs879255329
SNP Nexus

SNPshotrs879255329
SNPdbers879255329
MSV3drs879255329
GWAS Ctlgrs879255329
Max Magnitude0
ClinVar
Risk rs879255329(TT;TT)
Alt rs879255329(TT;TT)
Reference rs879255329(;)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA2
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.32913871_32913872insTT
CLNSRC
CLNACC RCV000239112.1,