Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507626(-;-)
Make rs397507626(-;A)
Make rs397507626(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336790
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507626
ebirs397507626
HLIrs397507626
Exacrs397507626
Varsomers397507626
Maprs397507626
PheGenIrs397507626
hapmaprs397507626
1000 genomesrs397507626
hgdprs397507626
ensemblrs397507626
gopubmedrs397507626
geneviewrs397507626
scholarrs397507626
googlers397507626
pharmgkbrs397507626
gwascentralrs397507626
openSNPrs397507626
23andMers397507626
23andMe allrs397507626
SNP Nexus

SNPshotrs397507626
SNPdbers397507626
MSV3drs397507626
GWAS Ctlgrs397507626
Max Magnitude0
ClinVar
Risk rs397507626(A;A)
Alt rs397507626(A;A)
Reference rs397507626(;)
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.32910927dupA
CLNSRC ClinVar
CLNACC RCV000043993.2, RCV000213096.1,