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rs397507989

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507989(-;-)
Make rs397507989(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370996
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507989
ebirs397507989
HLIrs397507989
Exacrs397507989
Varsomers397507989
Maprs397507989
PheGenIrs397507989
hapmaprs397507989
1000 genomesrs397507989
hgdprs397507989
ensemblrs397507989
gopubmedrs397507989
geneviewrs397507989
scholarrs397507989
googlers397507989
pharmgkbrs397507989
gwascentralrs397507989
openSNPrs397507989
23andMers397507989
23andMe allrs397507989
SNP Nexus

SNPshotrs397507989
SNPdbers397507989
MSV3drs397507989
GWAS Ctlgrs397507989
Max Magnitude0
ClinVar
Risk rs397507989(;)
Alt rs397507989(;)
Reference rs397507989(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.32945133delA
CLNSRC ClinVar
CLNACC RCV000045547.2,