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rs397507720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
(CA;CA) 0 common in clinvar
Make rs397507720(-;-)
Make rs397507720(-;CA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338819
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507720
ebirs397507720
HLIrs397507720
Exacrs397507720
Varsomers397507720
Maprs397507720
PheGenIrs397507720
hapmaprs397507720
1000 genomesrs397507720
hgdprs397507720
ensemblrs397507720
gopubmedrs397507720
geneviewrs397507720
scholarrs397507720
googlers397507720
pharmgkbrs397507720
gwascentralrs397507720
openSNPrs397507720
23andMers397507720
23andMe allrs397507720
SNP Nexus

SNPshotrs397507720
SNPdbers397507720
MSV3drs397507720
GWAS Ctlgrs397507720
Max Magnitude0
ClinVar
Risk rs397507720(;)
Alt rs397507720(;)
Reference rs397507720(AC;AC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912956_32912957delCA
CLNSRC ClinVar
CLNACC RCV000044418.2,