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rs786203843

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203843(-;-)
Make rs786203843(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32394694
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786203843
ebirs786203843
HLIrs786203843
Exacrs786203843
Varsomers786203843
Maprs786203843
PheGenIrs786203843
hapmaprs786203843
1000 genomesrs786203843
hgdprs786203843
ensemblrs786203843
gopubmedrs786203843
geneviewrs786203843
scholarrs786203843
googlers786203843
pharmgkbrs786203843
gwascentralrs786203843
openSNPrs786203843
23andMers786203843
23andMe allrs786203843
SNP Nexus

SNPshotrs786203843
SNPdbers786203843
MSV3drs786203843
GWAS Ctlgrs786203843
Max Magnitude0
ClinVar
Risk rs786203843(;)
Alt rs786203843(;)
Reference rs786203843(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32968831delG
CLNSRC
CLNACC RCV000167328.1,