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

rs786205482

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205482(C;C)
Make rs786205482(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32398615
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786205482
ebirs786205482
HLIrs786205482
Exacrs786205482
Varsomers786205482
Maprs786205482
PheGenIrs786205482
hapmaprs786205482
1000 genomesrs786205482
hgdprs786205482
ensemblrs786205482
gopubmedrs786205482
geneviewrs786205482
scholarrs786205482
googlers786205482
pharmgkbrs786205482
gwascentralrs786205482
openSNPrs786205482
23andMers786205482
23andMe allrs786205482
SNP Nexus

SNPshotrs786205482
SNPdbers786205482
MSV3drs786205482
GWAS Ctlgrs786205482
Max Magnitude0
ClinVar
Risk rs786205482(C;C)
Alt rs786205482(C;C)
Reference rs786205482(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32972752T>C
CLNSRC
CLNACC RCV000171217.1,