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rs397507957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507957(-;-)
Make rs397507957(-;GCAAAAAC)
Make rs397507957(GCAAAAAC;GCAAAAAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363256
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507957
ebirs397507957
HLIrs397507957
Exacrs397507957
Varsomers397507957
Maprs397507957
PheGenIrs397507957
hapmaprs397507957
1000 genomesrs397507957
hgdprs397507957
ensemblrs397507957
gopubmedrs397507957
geneviewrs397507957
scholarrs397507957
googlers397507957
pharmgkbrs397507957
gwascentralrs397507957
openSNPrs397507957
23andMers397507957
23andMe allrs397507957
SNP Nexus

SNPshotrs397507957
SNPdbers397507957
MSV3drs397507957
GWAS Ctlgrs397507957
Max Magnitude0
ClinVar
Risk rs397507957(GCAAAAAC;GCAAAAAC)
Alt rs397507957(GCAAAAAC;GCAAAAAC)
Reference rs397507957(;)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32937386_32937393dupGCAAAAAC
CLNSRC ClinVar
CLNACC RCV000045400.2, RCV000218114.1,