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rs397507888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507888(-;-)
Make rs397507888(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32346848
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507888
ebirs397507888
HLIrs397507888
Exacrs397507888
Varsomers397507888
Maprs397507888
PheGenIrs397507888
hapmaprs397507888
1000 genomesrs397507888
hgdprs397507888
ensemblrs397507888
gopubmedrs397507888
geneviewrs397507888
scholarrs397507888
googlers397507888
pharmgkbrs397507888
gwascentralrs397507888
openSNPrs397507888
23andMers397507888
23andMe allrs397507888
SNP Nexus

SNPshotrs397507888
SNPdbers397507888
MSV3drs397507888
GWAS Ctlgrs397507888
Max Magnitude0
ClinVar
Risk rs397507888(;)
Alt rs397507888(;)
Reference rs397507888(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32920985delT
CLNSRC ClinVar
CLNACC RCV000045099.2,