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rs864622134

From SNPedia

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


Make rs864622134(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32338004
GeneBRCA2
is asnp
is mentioned by
dbSNPrs864622134
dbSNP (old)rs864622134
ClinGenrs864622134
ebirs864622134
HLIrs864622134
Exacrs864622134
Varsomers864622134
Maprs864622134
PheGenIrs864622134
Biobankrs864622134
1000 genomesrs864622134
hgdprs864622134
ensemblrs864622134
gopubmedrs864622134
geneviewrs864622134
scholarrs864622134
googlers864622134
pharmgkbrs864622134
gwascentralrs864622134
openSNPrs864622134
23andMers864622134
23andMe allrs864622134
SNP Nexus

SNPshotrs864622134
SNPdbers864622134
MSV3drs864622134
GWAS Ctlgrs864622134
Max Magnitude6
ClinVar
Risk rs864622134(-;-)
Alt rs864622134(-;-)
Reference Rs864622134(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912141delA
CLNSRC
CLNACC RCV000203787.1, RCV000240988.1,