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rs397507356

From SNPedia

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


Make rs397507356(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339958
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507356
dbSNP (old)rs397507356
ClinGenrs397507356
ebirs397507356
HLIrs397507356
Exacrs397507356
Gnomadrs397507356
Varsomers397507356
Maprs397507356
PheGenIrs397507356
Biobankrs397507356
1000 genomesrs397507356
hgdprs397507356
ensemblrs397507356
gopubmedrs397507356
geneviewrs397507356
scholarrs397507356
googlers397507356
pharmgkbrs397507356
gwascentralrs397507356
openSNPrs397507356
23andMers397507356
23andMe allrs397507356
SNP Nexus

SNPshotrs397507356
SNPdbers397507356
MSV3drs397507356
GWAS Ctlgrs397507356
Max Magnitude6
ClinVar
Risk rs397507356(-;-)
Alt rs397507356(-;-)
Reference Rs397507356(ACAG;ACAG)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32914095_32914098delACAG
CLNSRC ClinVar
CLNACC RCV000031559.6, RCV000456296.1,