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rs753870552

From SNPedia

Orientationplus
Geno Mag Summary
(TACT;TACT) 0 common in clinvar
Make rs753870552(-;-)
Make rs753870552(-;TACT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339566
GeneBRCA2
is asnp
is mentioned by
dbSNPrs753870552
ebirs753870552
HLIrs753870552
Exacrs753870552
Varsomers753870552
Maprs753870552
PheGenIrs753870552
hapmaprs753870552
1000 genomesrs753870552
hgdprs753870552
ensemblrs753870552
gopubmedrs753870552
geneviewrs753870552
scholarrs753870552
googlers753870552
pharmgkbrs753870552
gwascentralrs753870552
openSNPrs753870552
23andMers753870552
23andMe allrs753870552
SNP Nexus

SNPshotrs753870552
SNPdbers753870552
MSV3drs753870552
GWAS Ctlgrs753870552
Max Magnitude0
ClinVar
Risk rs753870552(;)
Alt rs753870552(;)
Reference rs753870552(TACT;TACT)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32913705_32913708delCTTA
CLNSRC Breast Cancer Information Core (BRCA2) Inc.
CLNACC RCV000031532.4, RCV000044609.3, RCV000221073.1, RCV000234881.1,