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

rs397507818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507818(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340339
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507818
dbSNP (old)rs397507818
ClinGenrs397507818
ebirs397507818
HLIrs397507818
Exacrs397507818
Gnomadrs397507818
Varsomers397507818
Maprs397507818
PheGenIrs397507818
Biobankrs397507818
1000 genomesrs397507818
hgdprs397507818
ensemblrs397507818
gopubmedrs397507818
geneviewrs397507818
scholarrs397507818
googlers397507818
pharmgkbrs397507818
gwascentralrs397507818
openSNPrs397507818
23andMers397507818
23andMe allrs397507818
SNP Nexus

SNPshotrs397507818
SNPdbers397507818
MSV3drs397507818
GWAS Ctlgrs397507818
Max Magnitude6
ClinVar
Risk rs397507818(A;A)
Alt rs397507818(A;A)
Reference Rs397507818(-;-)
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.32914476dupA
CLNSRC ClinVar
CLNACC RCV000044812.3, RCV000257511.2,