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

rs397507300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs397507300(-;-)
Make rs397507300(-;CA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337364
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507300
ebirs397507300
HLIrs397507300
Exacrs397507300
Varsomers397507300
Maprs397507300
PheGenIrs397507300
hapmaprs397507300
1000 genomesrs397507300
hgdprs397507300
ensemblrs397507300
gopubmedrs397507300
geneviewrs397507300
scholarrs397507300
googlers397507300
pharmgkbrs397507300
gwascentralrs397507300
openSNPrs397507300
23andMers397507300
23andMe allrs397507300
SNP Nexus

SNPshotrs397507300
SNPdbers397507300
MSV3drs397507300
GWAS Ctlgrs397507300
Max Magnitude0
ClinVar
Risk rs397507300(;)
Alt rs397507300(;)
Reference rs397507300(CA;CA)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32911501_32911502delCA
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031395.3, RCV000132309.2, RCV000232051.1,