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rs276174844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTTTT;GTTTT) 0 common in clinvar
(TTTGT;TTTGT) 0 common in clinvar
Make rs276174844(-;-)
Make rs276174844(-;GTTTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326089
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174844
ebirs276174844
HLIrs276174844
Exacrs276174844
Varsomers276174844
Maprs276174844
PheGenIrs276174844
hapmaprs276174844
1000 genomesrs276174844
hgdprs276174844
ensemblrs276174844
gopubmedrs276174844
geneviewrs276174844
scholarrs276174844
googlers276174844
pharmgkbrs276174844
gwascentralrs276174844
openSNPrs276174844
23andMers276174844
23andMe allrs276174844
SNP Nexus

SNPshotrs276174844
SNPdbers276174844
MSV3drs276174844
GWAS Ctlgrs276174844
Max Magnitude0
ClinVar
Risk rs276174844(;)
Alt rs276174844(;)
Reference rs276174844(TTTGT;TTTGT)
Significance Probable-Pathogenic
Disease not provided Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN not provided Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32900226_32900230delGTTTT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044380.5, RCV000113566.1, RCV000203666.1,