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

rs786203680

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203680(G;G)
Make rs786203680(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32357842
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203680
ebirs786203680
HLIrs786203680
Exacrs786203680
Varsomers786203680
Maprs786203680
PheGenIrs786203680
hapmaprs786203680
1000 genomesrs786203680
hgdprs786203680
ensemblrs786203680
gopubmedrs786203680
geneviewrs786203680
scholarrs786203680
googlers786203680
pharmgkbrs786203680
gwascentralrs786203680
openSNPrs786203680
23andMers786203680
23andMe allrs786203680
SNP Nexus

SNPshotrs786203680
SNPdbers786203680
MSV3drs786203680
GWAS Ctlgrs786203680
Max Magnitude0
ClinVar
Risk rs786203680(G;G)
Alt rs786203680(G;G)
Reference rs786203680(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32931979T>G
CLNSRC
CLNACC RCV000167091.1,