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

rs397507721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507721(-;-)
Make rs397507721(-;A)
Make rs397507721(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338835
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507721
ebirs397507721
HLIrs397507721
Exacrs397507721
Varsomers397507721
Maprs397507721
PheGenIrs397507721
hapmaprs397507721
1000 genomesrs397507721
hgdprs397507721
ensemblrs397507721
gopubmedrs397507721
geneviewrs397507721
scholarrs397507721
googlers397507721
pharmgkbrs397507721
gwascentralrs397507721
openSNPrs397507721
23andMers397507721
23andMe allrs397507721
SNP Nexus

SNPshotrs397507721
SNPdbers397507721
MSV3drs397507721
GWAS Ctlgrs397507721
Max Magnitude0
ClinVar
Risk rs397507721(A;A)
Alt rs397507721(A;A)
Reference rs397507721(;)
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.32912972dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044422.2, RCV000113306.1,