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rs397507718

From SNPedia

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


Make rs397507718(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338764
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507718
dbSNP (old)rs397507718
ClinGenrs397507718
ebirs397507718
HLIrs397507718
Exacrs397507718
Gnomadrs397507718
Varsomers397507718
Maprs397507718
PheGenIrs397507718
Biobankrs397507718
1000 genomesrs397507718
hgdprs397507718
ensemblrs397507718
gopubmedrs397507718
geneviewrs397507718
scholarrs397507718
googlers397507718
pharmgkbrs397507718
gwascentralrs397507718
openSNPrs397507718
23andMers397507718
23andMe allrs397507718
SNP Nexus

SNPshotrs397507718
SNPdbers397507718
MSV3drs397507718
GWAS Ctlgrs397507718
Max Magnitude6
ClinVar
Risk rs397507718(-;-)
Alt rs397507718(-;-)
Reference Rs397507718(ATAAG;ATAAG)
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.32912901_32912905delTAAGA
CLNSRC ClinVar
CLNACC RCV000044407.3, RCV000238723.3,