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rs397507855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATC;AATC) 0 common in clinvar
(ATCA;ATCA) 0 common in clinvar
Make rs397507855(-;-)
Make rs397507855(-;ATCA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340792
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507855
ebirs397507855
HLIrs397507855
Exacrs397507855
Varsomers397507855
Maprs397507855
PheGenIrs397507855
hapmaprs397507855
1000 genomesrs397507855
hgdprs397507855
ensemblrs397507855
gopubmedrs397507855
geneviewrs397507855
scholarrs397507855
googlers397507855
pharmgkbrs397507855
gwascentralrs397507855
openSNPrs397507855
23andMers397507855
23andMe allrs397507855
SNP Nexus

SNPshotrs397507855
SNPdbers397507855
MSV3drs397507855
GWAS Ctlgrs397507855
Max Magnitude0
ClinVar
Risk rs397507855(;)
Alt rs397507855(;)
Reference rs397507855(AATC;AATC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914929_32914932delATCA
CLNSRC ClinVar
CLNACC RCV000044947.2,