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rs397508032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGAGCTAACATACAG;AAGAGCTAACATACAG) 0 common in clinvar
Make rs397508032(-;-)
Make rs397508032(-;AAGAGCTAACATACAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379859
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508032
ebirs397508032
HLIrs397508032
Exacrs397508032
Varsomers397508032
Maprs397508032
PheGenIrs397508032
hapmaprs397508032
1000 genomesrs397508032
hgdprs397508032
ensemblrs397508032
gopubmedrs397508032
geneviewrs397508032
scholarrs397508032
googlers397508032
pharmgkbrs397508032
gwascentralrs397508032
openSNPrs397508032
23andMers397508032
23andMe allrs397508032
SNP Nexus

SNPshotrs397508032
SNPdbers397508032
MSV3drs397508032
GWAS Ctlgrs397508032
Max Magnitude0
ClinVar
Risk rs397508032(;)
Alt rs397508032(;)
Reference rs397508032(AAGAGCTAACATACAG;AAGAGCTAACATACAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953996_32954011del16
CLNSRC ClinVar
CLNACC RCV000045701.2,