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rs879255331

From SNPedia

Orientationplus
Geno Mag Summary
(TCTTTCCACAGCCA;TCTTTCCACAGCCA) 0 common in clinvar
Make rs879255331(G;G)
Make rs879255331(G;TCTTTCCACAGCCA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32356500
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255331
ebirs879255331
HLIrs879255331
Exacrs879255331
Varsomers879255331
Maprs879255331
PheGenIrs879255331
hapmaprs879255331
1000 genomesrs879255331
hgdprs879255331
ensemblrs879255331
gopubmedrs879255331
geneviewrs879255331
scholarrs879255331
googlers879255331
pharmgkbrs879255331
gwascentralrs879255331
openSNPrs879255331
23andMers879255331
23andMe allrs879255331
SNP Nexus

SNPshotrs879255331
SNPdbers879255331
MSV3drs879255331
GWAS Ctlgrs879255331
Max Magnitude0
ClinVar
Risk rs879255331(G;G)
Alt rs879255331(G;G)
Reference rs879255331(TCTTTCCACAGCCA;TCTTTCCACAGCCA)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32930637_32930650delTCTTTCCACAGCCAinsG
CLNSRC
CLNACC RCV000238954.1,