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

rs397507803

From SNPedia

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


Make rs397507803(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340109
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507803
dbSNP (old)rs397507803
ClinGenrs397507803
ebirs397507803
HLIrs397507803
Exacrs397507803
Gnomadrs397507803
Varsomers397507803
Maprs397507803
PheGenIrs397507803
Biobankrs397507803
1000 genomesrs397507803
hgdprs397507803
ensemblrs397507803
gopubmedrs397507803
geneviewrs397507803
scholarrs397507803
googlers397507803
pharmgkbrs397507803
gwascentralrs397507803
openSNPrs397507803
23andMers397507803
23andMe allrs397507803
SNP Nexus

SNPshotrs397507803
SNPdbers397507803
MSV3drs397507803
GWAS Ctlgrs397507803
Max Magnitude6
ClinVar
Risk rs397507803(-;-) Rs397507803(AT;AT)
Alt rs397507803(-;-) Rs397507803(AT;AT)
Reference Rs397507803(TA;TA)
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.32914246_32914247delTA
CLNSRC ClinVar
CLNACC RCV000044745.2, RCV000241337.2,