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rs786204281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs786204281(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32355193
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786204281
ClinGenrs786204281
ebirs786204281
HLIrs786204281
Exacrs786204281
Varsomers786204281
Maprs786204281
PheGenIrs786204281
hapmaprs786204281
1000 genomesrs786204281
hgdprs786204281
ensemblrs786204281
gopubmedrs786204281
geneviewrs786204281
scholarrs786204281
googlers786204281
pharmgkbrs786204281
gwascentralrs786204281
openSNPrs786204281
23andMers786204281
23andMe allrs786204281
SNP Nexus

SNPshotrs786204281
SNPdbers786204281
MSV3drs786204281
GWAS Ctlgrs786204281
Max Magnitude6
ClinVar
Risk rs786204281(A;A)
Alt rs786204281(A;A)
Reference Rs786204281(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32929330dupA
CLNSRC
CLNACC RCV000168596.3,