Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508010

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
(GAAA;GAAA) 0 common in clinvar
Make rs397508010(-;-)
Make rs397508010(-;GAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379379
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508010
ebirs397508010
HLIrs397508010
Exacrs397508010
Varsomers397508010
Maprs397508010
PheGenIrs397508010
hapmaprs397508010
1000 genomesrs397508010
hgdprs397508010
ensemblrs397508010
gopubmedrs397508010
geneviewrs397508010
scholarrs397508010
googlers397508010
pharmgkbrs397508010
gwascentralrs397508010
openSNPrs397508010
23andMers397508010
23andMe allrs397508010
SNP Nexus

SNPshotrs397508010
SNPdbers397508010
MSV3drs397508010
GWAS Ctlgrs397508010
Max Magnitude0
ClinVar
Risk rs397508010(;)
Alt rs397508010(;)
Reference rs397508010(AAGA;AAGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953516_32953519delGAAA
CLNSRC ClinVar
CLNACC RCV000045633.2,