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

rs398122790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs398122790(-;-)
Make rs398122790(-;AT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339345
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122790
ebirs398122790
HLIrs398122790
Exacrs398122790
Varsomers398122790
Maprs398122790
PheGenIrs398122790
hapmaprs398122790
1000 genomesrs398122790
hgdprs398122790
ensemblrs398122790
gopubmedrs398122790
geneviewrs398122790
scholarrs398122790
googlers398122790
pharmgkbrs398122790
gwascentralrs398122790
openSNPrs398122790
23andMers398122790
23andMe allrs398122790
SNP Nexus

SNPshotrs398122790
SNPdbers398122790
MSV3drs398122790
GWAS Ctlgrs398122790
Max Magnitude0
ClinVar
Risk rs398122790(;)
Alt rs398122790(;)
Reference rs398122790(AT;AT)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913482_32913483delAT
CLNSRC ClinVar
CLNACC RCV000077739.2,