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rs397507786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507786(-;-)
Make rs397507786(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339826
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507786
ClinGenrs397507786
ebirs397507786
HLIrs397507786
Exacrs397507786
Varsomers397507786
Maprs397507786
PheGenIrs397507786
hapmaprs397507786
1000 genomesrs397507786
hgdprs397507786
ensemblrs397507786
gopubmedrs397507786
geneviewrs397507786
scholarrs397507786
googlers397507786
pharmgkbrs397507786
gwascentralrs397507786
openSNPrs397507786
23andMers397507786
23andMe allrs397507786
SNP Nexus

SNPshotrs397507786
SNPdbers397507786
MSV3drs397507786
GWAS Ctlgrs397507786
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397507786(A;A)
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.32913963delA
CLNSRC ClinVar
CLNACC RCV000044667.2, RCV000257292.2,