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rs397507784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGGA;AGGA) 0 common in clinvar
(GGAA;GGAA) 0 common in clinvar
Make rs397507784(-;-)
Make rs397507784(-;GGAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339788
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507784
ebirs397507784
HLIrs397507784
Exacrs397507784
Varsomers397507784
Maprs397507784
PheGenIrs397507784
hapmaprs397507784
1000 genomesrs397507784
hgdprs397507784
ensemblrs397507784
gopubmedrs397507784
geneviewrs397507784
scholarrs397507784
googlers397507784
pharmgkbrs397507784
gwascentralrs397507784
openSNPrs397507784
23andMers397507784
23andMe allrs397507784
SNP Nexus

SNPshotrs397507784
SNPdbers397507784
MSV3drs397507784
GWAS Ctlgrs397507784
Max Magnitude0
ClinVar
Risk rs397507784(;)
Alt rs397507784(;)
Reference rs397507784(AGGA;AGGA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913925_32913928delGGAA
CLNSRC ClinVar
CLNACC RCV000044659.2,