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rs397507817

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs397507817(-;-)
Make rs397507817(-;AT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340319
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507817
ebirs397507817
HLIrs397507817
Exacrs397507817
Varsomers397507817
Maprs397507817
PheGenIrs397507817
hapmaprs397507817
1000 genomesrs397507817
hgdprs397507817
ensemblrs397507817
gopubmedrs397507817
geneviewrs397507817
scholarrs397507817
googlers397507817
pharmgkbrs397507817
gwascentralrs397507817
openSNPrs397507817
23andMers397507817
23andMe allrs397507817
SNP Nexus

SNPshotrs397507817
SNPdbers397507817
MSV3drs397507817
GWAS Ctlgrs397507817
Max Magnitude0
ClinVar
Risk rs397507817(;)
Alt rs397507817(;)
Reference rs397507817(TA;TA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914456_32914457delAT
CLNSRC ClinVar
CLNACC RCV000044805.2,