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

rs786204209

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204209(-;-)
Make rs786204209(-;C)
Make rs786204209(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339046
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786204209
ebirs786204209
HLIrs786204209
Exacrs786204209
Varsomers786204209
Maprs786204209
PheGenIrs786204209
hapmaprs786204209
1000 genomesrs786204209
hgdprs786204209
ensemblrs786204209
gopubmedrs786204209
geneviewrs786204209
scholarrs786204209
googlers786204209
pharmgkbrs786204209
gwascentralrs786204209
openSNPrs786204209
23andMers786204209
23andMe allrs786204209
SNP Nexus

SNPshotrs786204209
SNPdbers786204209
MSV3drs786204209
GWAS Ctlgrs786204209
Max Magnitude0
ClinVar
Risk rs786204209(C;C)
Alt rs786204209(C;C)
Reference rs786204209(;)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32913183dupC
CLNSRC
CLNACC RCV000168306.2,