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rs397507707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507707(-;-)
Make rs397507707(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338476
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507707
ebirs397507707
HLIrs397507707
Exacrs397507707
Varsomers397507707
Maprs397507707
PheGenIrs397507707
hapmaprs397507707
1000 genomesrs397507707
hgdprs397507707
ensemblrs397507707
gopubmedrs397507707
geneviewrs397507707
scholarrs397507707
googlers397507707
pharmgkbrs397507707
gwascentralrs397507707
openSNPrs397507707
23andMers397507707
23andMe allrs397507707
SNP Nexus

SNPshotrs397507707
SNPdbers397507707
MSV3drs397507707
GWAS Ctlgrs397507707
Max Magnitude0
ClinVar
Risk rs397507707(;)
Alt rs397507707(;)
Reference rs397507707(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912613delA
CLNSRC ClinVar
CLNACC RCV000044354.2,