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rs397507808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs397507808(-;-)
Make rs397507808(-;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340184
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507808
ebirs397507808
HLIrs397507808
Exacrs397507808
Varsomers397507808
Maprs397507808
PheGenIrs397507808
hapmaprs397507808
1000 genomesrs397507808
hgdprs397507808
ensemblrs397507808
gopubmedrs397507808
geneviewrs397507808
scholarrs397507808
googlers397507808
pharmgkbrs397507808
gwascentralrs397507808
openSNPrs397507808
23andMers397507808
23andMe allrs397507808
SNP Nexus

SNPshotrs397507808
SNPdbers397507808
MSV3drs397507808
GWAS Ctlgrs397507808
Max Magnitude0
ClinVar
Risk rs397507808(;)
Alt rs397507808(;)
Reference rs397507808(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.32914321_32914322delTA
CLNSRC ClinVar
CLNACC RCV000044767.2,