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rs397507597

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397507597(-;-)
Make rs397507597(-;AG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333090
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507597
ebirs397507597
HLIrs397507597
Exacrs397507597
Varsomers397507597
Maprs397507597
PheGenIrs397507597
hapmaprs397507597
1000 genomesrs397507597
hgdprs397507597
ensemblrs397507597
gopubmedrs397507597
geneviewrs397507597
scholarrs397507597
googlers397507597
pharmgkbrs397507597
gwascentralrs397507597
openSNPrs397507597
23andMers397507597
23andMe allrs397507597
SNP Nexus

SNPshotrs397507597
SNPdbers397507597
MSV3drs397507597
GWAS Ctlgrs397507597
Max Magnitude0
ClinVar
Risk rs397507597(;)
Alt rs397507597(;)
Reference rs397507597(AG;AG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907227_32907228delAG
CLNSRC ClinVar
CLNACC RCV000043842.2,