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rs786204283

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204283(C;G)
Make rs786204283(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32394713
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786204283
ebirs786204283
HLIrs786204283
Exacrs786204283
Varsomers786204283
Maprs786204283
PheGenIrs786204283
hapmaprs786204283
1000 genomesrs786204283
hgdprs786204283
ensemblrs786204283
gopubmedrs786204283
geneviewrs786204283
scholarrs786204283
googlers786204283
pharmgkbrs786204283
gwascentralrs786204283
openSNPrs786204283
23andMers786204283
23andMe allrs786204283
SNP Nexus

SNPshotrs786204283
SNPdbers786204283
MSV3drs786204283
GWAS Ctlgrs786204283
Max Magnitude0
ClinVar
Risk rs786204283(G;G)
Alt rs786204283(G;G)
Reference rs786204283(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32968850C>G
CLNSRC
CLNACC RCV000168614.1,