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rs879255325

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255325(A;T)
Make rs879255325(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333066
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255325
ebirs879255325
HLIrs879255325
Exacrs879255325
Varsomers879255325
Maprs879255325
PheGenIrs879255325
hapmaprs879255325
1000 genomesrs879255325
hgdprs879255325
ensemblrs879255325
gopubmedrs879255325
geneviewrs879255325
scholarrs879255325
googlers879255325
pharmgkbrs879255325
gwascentralrs879255325
openSNPrs879255325
23andMers879255325
23andMe allrs879255325
SNP Nexus

SNPshotrs879255325
SNPdbers879255325
MSV3drs879255325
GWAS Ctlgrs879255325
Max Magnitude0
ClinVar
Risk rs879255325(T;T)
Alt rs879255325(T;T)
Reference rs879255325(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BRCA2
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.32907203A>T
CLNSRC
CLNACC RCV000239040.1,