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rs397508015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGG;AAGG) 0 common in clinvar
(AGGA;AGGA) 0 common in clinvar
Make rs397508015(-;-)
Make rs397508015(-;AAGG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379410
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508015
ebirs397508015
HLIrs397508015
Exacrs397508015
Varsomers397508015
Maprs397508015
PheGenIrs397508015
hapmaprs397508015
1000 genomesrs397508015
hgdprs397508015
ensemblrs397508015
gopubmedrs397508015
geneviewrs397508015
scholarrs397508015
googlers397508015
pharmgkbrs397508015
gwascentralrs397508015
openSNPrs397508015
23andMers397508015
23andMe allrs397508015
SNP Nexus

SNPshotrs397508015
SNPdbers397508015
MSV3drs397508015
GWAS Ctlgrs397508015
Max Magnitude0
ClinVar
Risk rs397508015(;)
Alt rs397508015(;)
Reference rs397508015(AGGA;AGGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953547_32953550delAAGG
CLNSRC ClinVar
CLNACC RCV000045640.2,