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rs397508011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAC;AAAC) 0 common in clinvar
(ACAA;ACAA) 0 common in clinvar
Make rs397508011(-;-)
Make rs397508011(-;ACAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379382
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508011
ebirs397508011
HLIrs397508011
Exacrs397508011
Varsomers397508011
Maprs397508011
PheGenIrs397508011
hapmaprs397508011
1000 genomesrs397508011
hgdprs397508011
ensemblrs397508011
gopubmedrs397508011
geneviewrs397508011
scholarrs397508011
googlers397508011
pharmgkbrs397508011
gwascentralrs397508011
openSNPrs397508011
23andMers397508011
23andMe allrs397508011
SNP Nexus

SNPshotrs397508011
SNPdbers397508011
MSV3drs397508011
GWAS Ctlgrs397508011
Max Magnitude0
ClinVar
Risk rs397508011(;)
Alt rs397508011(;)
Reference rs397508011(AAAC;AAAC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953519_32953522delACAA
CLNSRC ClinVar
CLNACC RCV000045634.2,