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rs397507816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507816(-;-)
Make rs397507816(-;GCTAC)
Make rs397507816(GCTAC;GCTAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326581
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507816
ebirs397507816
HLIrs397507816
Exacrs397507816
Varsomers397507816
Maprs397507816
PheGenIrs397507816
hapmaprs397507816
1000 genomesrs397507816
hgdprs397507816
ensemblrs397507816
gopubmedrs397507816
geneviewrs397507816
scholarrs397507816
googlers397507816
pharmgkbrs397507816
gwascentralrs397507816
openSNPrs397507816
23andMers397507816
23andMe allrs397507816
SNP Nexus

SNPshotrs397507816
SNPdbers397507816
MSV3drs397507816
GWAS Ctlgrs397507816
Max Magnitude0
ClinVar
Risk rs397507816(GCTAC;GCTAC)
Alt rs397507816(GCTAC;GCTAC)
Reference rs397507816(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900714_32900718dupGCTAC
CLNSRC ClinVar
CLNACC RCV000044804.2,