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rs786204278

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204278(-;-)
Make rs786204278(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340529
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786204278
ebirs786204278
HLIrs786204278
Exacrs786204278
Varsomers786204278
Maprs786204278
PheGenIrs786204278
hapmaprs786204278
1000 genomesrs786204278
hgdprs786204278
ensemblrs786204278
gopubmedrs786204278
geneviewrs786204278
scholarrs786204278
googlers786204278
pharmgkbrs786204278
gwascentralrs786204278
openSNPrs786204278
23andMers786204278
23andMe allrs786204278
SNP Nexus

SNPshotrs786204278
SNPdbers786204278
MSV3drs786204278
GWAS Ctlgrs786204278
Max Magnitude0
ClinVar
Risk rs786204278(;)
Alt rs786204278(;)
Reference rs786204278(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914666delT
CLNSRC
CLNACC RCV000168588.1,