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rs397507633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
(GAAA;GAAA) 0 common in clinvar
Make rs397507633(-;-)
Make rs397507633(-;GAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336951
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507633
ebirs397507633
HLIrs397507633
Exacrs397507633
Varsomers397507633
Maprs397507633
PheGenIrs397507633
hapmaprs397507633
1000 genomesrs397507633
hgdprs397507633
ensemblrs397507633
gopubmedrs397507633
geneviewrs397507633
scholarrs397507633
googlers397507633
pharmgkbrs397507633
gwascentralrs397507633
openSNPrs397507633
23andMers397507633
23andMe allrs397507633
SNP Nexus

SNPshotrs397507633
SNPdbers397507633
MSV3drs397507633
GWAS Ctlgrs397507633
Max Magnitude0
ClinVar
Risk rs397507633(;)
Alt rs397507633(;)
Reference rs397507633(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.32911088_32911091delGAAA
CLNSRC ClinVar
CLNACC RCV000044022.2,