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rs397507870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAAGTTT;AGAAGTTT) 0 common in clinvar
(TAGAAGTT;TAGAAGTT) 0 common in clinvar
Make rs397507870(-;-)
Make rs397507870(-;AGAAGTTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340982
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507870
ebirs397507870
HLIrs397507870
Exacrs397507870
Varsomers397507870
Maprs397507870
PheGenIrs397507870
hapmaprs397507870
1000 genomesrs397507870
hgdprs397507870
ensemblrs397507870
gopubmedrs397507870
geneviewrs397507870
scholarrs397507870
googlers397507870
pharmgkbrs397507870
gwascentralrs397507870
openSNPrs397507870
23andMers397507870
23andMe allrs397507870
SNP Nexus

SNPshotrs397507870
SNPdbers397507870
MSV3drs397507870
GWAS Ctlgrs397507870
Max Magnitude0
ClinVar
Risk rs397507870(;)
Alt rs397507870(;)
Reference rs397507870(TAGAAGTT;TAGAAGTT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32915119_32915126delAGAAGTTT
CLNSRC ClinVar
CLNACC RCV000044995.2,