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rs483353111

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483353111(-;-)
Make rs483353111(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32336950
GeneBRCA2
is asnp
is mentioned by
dbSNPrs483353111
ebirs483353111
HLIrs483353111
Exacrs483353111
Varsomers483353111
Maprs483353111
PheGenIrs483353111
hapmaprs483353111
1000 genomesrs483353111
hgdprs483353111
ensemblrs483353111
gopubmedrs483353111
geneviewrs483353111
scholarrs483353111
googlers483353111
pharmgkbrs483353111
gwascentralrs483353111
openSNPrs483353111
23andMers483353111
23andMe allrs483353111
SNP Nexus

SNPshotrs483353111
SNPdbers483353111
MSV3drs483353111
GWAS Ctlgrs483353111
Max Magnitude0
ClinVar
Risk rs483353111(;)
Alt rs483353111(;)
Reference rs483353111(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911087delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113067.1,