Have questions? Visit https://www.reddit.com/r/SNPedia

rs864622672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs864622672(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32337556
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622672
dbSNP (old)rs864622672
ClinGenrs864622672
ebirs864622672
HLIrs864622672
Exacrs864622672
Gnomadrs864622672
Varsomers864622672
Maprs864622672
PheGenIrs864622672
Biobankrs864622672
1000 genomesrs864622672
hgdprs864622672
ensemblrs864622672
gopubmedrs864622672
geneviewrs864622672
scholarrs864622672
googlers864622672
pharmgkbrs864622672
gwascentralrs864622672
openSNPrs864622672
23andMers864622672
23andMe allrs864622672
SNP Nexus

SNPshotrs864622672
SNPdbers864622672
MSV3drs864622672
GWAS Ctlgrs864622672
Max Magnitude6
ClinVar
Risk rs864622672(-;-)
Alt rs864622672(-;-)
Reference Rs864622672(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911693delT
CLNSRC
CLNACC RCV000206548.1, RCV000221184.1, RCV000238697.2,