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rs786202353

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786202353(-;-)
Make rs786202353(-;T)
Make rs786202353(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32379792
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202353
ebirs786202353
HLIrs786202353
Exacrs786202353
Varsomers786202353
Maprs786202353
PheGenIrs786202353
hapmaprs786202353
1000 genomesrs786202353
hgdprs786202353
ensemblrs786202353
gopubmedrs786202353
geneviewrs786202353
scholarrs786202353
googlers786202353
pharmgkbrs786202353
gwascentralrs786202353
openSNPrs786202353
23andMers786202353
23andMe allrs786202353
SNP Nexus

SNPshotrs786202353
SNPdbers786202353
MSV3drs786202353
GWAS Ctlgrs786202353
Max Magnitude0
ClinVar
Risk rs786202353(T;T)
Alt rs786202353(T;T)
Reference rs786202353(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953929dupT
CLNSRC
CLNACC RCV000165118.1,