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rs397507942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs397507942(-;-)
Make rs397507942(-;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362589
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507942
ebirs397507942
HLIrs397507942
Exacrs397507942
Varsomers397507942
Maprs397507942
PheGenIrs397507942
hapmaprs397507942
1000 genomesrs397507942
hgdprs397507942
ensemblrs397507942
gopubmedrs397507942
geneviewrs397507942
scholarrs397507942
googlers397507942
pharmgkbrs397507942
gwascentralrs397507942
openSNPrs397507942
23andMers397507942
23andMe allrs397507942
SNP Nexus

SNPshotrs397507942
SNPdbers397507942
MSV3drs397507942
GWAS Ctlgrs397507942
Max Magnitude0
ClinVar
Risk rs397507942(;)
Alt rs397507942(;)
Reference rs397507942(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.32936726_32936727delTA
CLNSRC ClinVar
CLNACC RCV000045334.2,