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rs397507700

From SNPedia

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


Make rs397507700(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338291
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507700
dbSNP (old)rs397507700
ClinGenrs397507700
ebirs397507700
HLIrs397507700
Exacrs397507700
Varsomers397507700
Maprs397507700
PheGenIrs397507700
Biobankrs397507700
1000 genomesrs397507700
hgdprs397507700
ensemblrs397507700
gopubmedrs397507700
geneviewrs397507700
scholarrs397507700
googlers397507700
pharmgkbrs397507700
gwascentralrs397507700
openSNPrs397507700
23andMers397507700
23andMe allrs397507700
SNP Nexus

SNPshotrs397507700
SNPdbers397507700
MSV3drs397507700
GWAS Ctlgrs397507700
Max Magnitude6
ClinVar
Risk rs397507700(-;-)
Alt rs397507700(-;-)
Reference Rs397507700(AATTACAAGAGAAATACTG;AATTACAAGAGAAATACTG)
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.32912428_32912446del19
CLNSRC ClinVar
CLNACC RCV000044314.2, RCV000257715.2,