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rs397508053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTTCA;TTTCA) 0 common in clinvar
Make rs397508053(GAATGATC;GAATGATC)
Make rs397508053(GAATGATC;TTTCA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394895
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508053
ebirs397508053
HLIrs397508053
Exacrs397508053
Varsomers397508053
Maprs397508053
PheGenIrs397508053
hapmaprs397508053
1000 genomesrs397508053
hgdprs397508053
ensemblrs397508053
gopubmedrs397508053
geneviewrs397508053
scholarrs397508053
googlers397508053
pharmgkbrs397508053
gwascentralrs397508053
openSNPrs397508053
23andMers397508053
23andMe allrs397508053
SNP Nexus

SNPshotrs397508053
SNPdbers397508053
MSV3drs397508053
GWAS Ctlgrs397508053
Max Magnitude0
ClinVar
Risk rs397508053(GAATGATC;GAATGATC)
Alt rs397508053(GAATGATC;GAATGATC)
Reference rs397508053(TTTCA;TTTCA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32969032_32969036delTTTCAinsGAATGATC
CLNSRC ClinVar
CLNACC RCV000045827.2,