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rs397507899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507899(-;-)
Make rs397507899(-;A)
Make rs397507899(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355030
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507899
ebirs397507899
HLIrs397507899
Exacrs397507899
Varsomers397507899
Maprs397507899
PheGenIrs397507899
hapmaprs397507899
1000 genomesrs397507899
hgdprs397507899
ensemblrs397507899
gopubmedrs397507899
geneviewrs397507899
scholarrs397507899
googlers397507899
pharmgkbrs397507899
gwascentralrs397507899
openSNPrs397507899
23andMers397507899
23andMe allrs397507899
SNP Nexus

SNPshotrs397507899
SNPdbers397507899
MSV3drs397507899
GWAS Ctlgrs397507899
Max Magnitude0
ClinVar
Risk rs397507899(A;A)
Alt rs397507899(A;A)
Reference rs397507899(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929167dupA
CLNSRC ClinVar
CLNACC RCV000045155.2,