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rs397507578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507578(-;-)
Make rs397507578(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332788
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507578
ebirs397507578
HLIrs397507578
Exacrs397507578
Varsomers397507578
Maprs397507578
PheGenIrs397507578
hapmaprs397507578
1000 genomesrs397507578
hgdprs397507578
ensemblrs397507578
gopubmedrs397507578
geneviewrs397507578
scholarrs397507578
googlers397507578
pharmgkbrs397507578
gwascentralrs397507578
openSNPrs397507578
23andMers397507578
23andMe allrs397507578
SNP Nexus

SNPshotrs397507578
SNPdbers397507578
MSV3drs397507578
GWAS Ctlgrs397507578
Max Magnitude0
ClinVar
Risk rs397507578(;)
Alt rs397507578(;)
Reference rs397507578(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906925_32906926delAA
CLNSRC ClinVar
CLNACC RCV000043778.2,