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

rs397507780

From SNPedia

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


Make rs397507780(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339708
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507780
dbSNP (old)rs397507780
ClinGenrs397507780
ebirs397507780
HLIrs397507780
Exacrs397507780
Gnomadrs397507780
Varsomers397507780
Maprs397507780
PheGenIrs397507780
Biobankrs397507780
1000 genomesrs397507780
hgdprs397507780
ensemblrs397507780
gopubmedrs397507780
geneviewrs397507780
scholarrs397507780
googlers397507780
pharmgkbrs397507780
gwascentralrs397507780
openSNPrs397507780
23andMers397507780
23andMe allrs397507780
SNP Nexus

SNPshotrs397507780
SNPdbers397507780
MSV3drs397507780
GWAS Ctlgrs397507780
Max Magnitude6
ClinVar
Risk rs397507780(-;-)
Alt rs397507780(-;-)
Reference Rs397507780(AC;AC)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913845_32913846delAC
CLNSRC ClinVar
CLNACC RCV000044643.2, RCV000257574.2,