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

rs786202461

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202461(A;A)
Make rs786202461(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340510
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202461
ebirs786202461
HLIrs786202461
Exacrs786202461
Varsomers786202461
Maprs786202461
PheGenIrs786202461
hapmaprs786202461
1000 genomesrs786202461
hgdprs786202461
ensemblrs786202461
gopubmedrs786202461
geneviewrs786202461
scholarrs786202461
googlers786202461
pharmgkbrs786202461
gwascentralrs786202461
openSNPrs786202461
23andMers786202461
23andMe allrs786202461
SNP Nexus

SNPshotrs786202461
SNPdbers786202461
MSV3drs786202461
GWAS Ctlgrs786202461
Max Magnitude0
ClinVar
Risk rs786202461(A;A)
Alt rs786202461(A;A)
Reference rs786202461(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914647C>A
CLNSRC
CLNACC RCV000165281.1,