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rs397507857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs397507857(-;-)
Make rs397507857(-;TA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340802
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507857
ebirs397507857
HLIrs397507857
Exacrs397507857
Varsomers397507857
Maprs397507857
PheGenIrs397507857
hapmaprs397507857
1000 genomesrs397507857
hgdprs397507857
ensemblrs397507857
gopubmedrs397507857
geneviewrs397507857
scholarrs397507857
googlers397507857
pharmgkbrs397507857
gwascentralrs397507857
openSNPrs397507857
23andMers397507857
23andMe allrs397507857
SNP Nexus

SNPshotrs397507857
SNPdbers397507857
MSV3drs397507857
GWAS Ctlgrs397507857
Max Magnitude0
ClinVar
Risk rs397507857(;)
Alt rs397507857(;)
Reference rs397507857(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.32914939_32914940delTA
CLNSRC ClinVar
CLNACC RCV000044956.2,