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rs397508041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs397508041(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380142
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508041
ClinGenrs397508041
ebirs397508041
HLIrs397508041
Exacrs397508041
Varsomers397508041
Maprs397508041
PheGenIrs397508041
hapmaprs397508041
1000 genomesrs397508041
hgdprs397508041
ensemblrs397508041
gopubmedrs397508041
geneviewrs397508041
scholarrs397508041
googlers397508041
pharmgkbrs397508041
gwascentralrs397508041
openSNPrs397508041
23andMers397508041
23andMe allrs397508041
SNP Nexus

SNPshotrs397508041
SNPdbers397508041
MSV3drs397508041
GWAS Ctlgrs397508041
Max Magnitude6
ClinVar
Risk rs397508041(-;-)
Alt rs397508041(-;-)
Reference Rs397508041(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome not provided Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome not provided Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32954279delA
CLNSRC ClinVar
CLNACC RCV000045759.3, RCV000236478.2, RCV000257577.2,