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rs397507570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507570(-;-)
Make rs397507570(-;T)
Make rs397507570(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332575
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507570
ebirs397507570
HLIrs397507570
Exacrs397507570
Varsomers397507570
Maprs397507570
PheGenIrs397507570
hapmaprs397507570
1000 genomesrs397507570
hgdprs397507570
ensemblrs397507570
gopubmedrs397507570
geneviewrs397507570
scholarrs397507570
googlers397507570
pharmgkbrs397507570
gwascentralrs397507570
openSNPrs397507570
23andMers397507570
23andMe allrs397507570
SNP Nexus

SNPshotrs397507570
SNPdbers397507570
MSV3drs397507570
GWAS Ctlgrs397507570
Max Magnitude0
ClinVar
Risk rs397507570(T;T)
Alt rs397507570(T;T)
Reference rs397507570(;)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906712dupT
CLNSRC ClinVar
CLNACC RCV000043736.2, RCV000225491.1,