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rs397507958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507958(-;-)
Make rs397507958(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363255
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507958
ebirs397507958
HLIrs397507958
Exacrs397507958
Varsomers397507958
Maprs397507958
PheGenIrs397507958
hapmaprs397507958
1000 genomesrs397507958
hgdprs397507958
ensemblrs397507958
gopubmedrs397507958
geneviewrs397507958
scholarrs397507958
googlers397507958
pharmgkbrs397507958
gwascentralrs397507958
openSNPrs397507958
23andMers397507958
23andMe allrs397507958
SNP Nexus

SNPshotrs397507958
SNPdbers397507958
MSV3drs397507958
GWAS Ctlgrs397507958
Max Magnitude0
ClinVar
Risk rs397507958(;)
Alt rs397507958(;)
Reference rs397507958(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.32937392delA
CLNSRC ClinVar
CLNACC RCV000045402.2,