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rs397508010

From SNPedia

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


Make rs397508010(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379379
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508010
dbSNP (old)rs397508010
ClinGenrs397508010
ebirs397508010
HLIrs397508010
Exacrs397508010
Gnomadrs397508010
Varsomers397508010
Maprs397508010
PheGenIrs397508010
Biobankrs397508010
1000 genomesrs397508010
hgdprs397508010
ensemblrs397508010
gopubmedrs397508010
geneviewrs397508010
scholarrs397508010
googlers397508010
pharmgkbrs397508010
gwascentralrs397508010
openSNPrs397508010
23andMers397508010
23andMe allrs397508010
SNP Nexus

SNPshotrs397508010
SNPdbers397508010
MSV3drs397508010
GWAS Ctlgrs397508010
Max Magnitude6
ClinVar
Risk rs397508010(-;-)
Alt rs397508010(-;-)
Reference Rs397508010(AAGA;AAGA)
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.32953516_32953519delGAAA
CLNSRC ClinVar
CLNACC RCV000045633.2, RCV000257676.2,