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rs786202756

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202756(-;-)
Make rs786202756(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32333333
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202756
ebirs786202756
HLIrs786202756
Exacrs786202756
Varsomers786202756
Maprs786202756
PheGenIrs786202756
hapmaprs786202756
1000 genomesrs786202756
hgdprs786202756
ensemblrs786202756
gopubmedrs786202756
geneviewrs786202756
scholarrs786202756
googlers786202756
pharmgkbrs786202756
gwascentralrs786202756
openSNPrs786202756
23andMers786202756
23andMe allrs786202756
SNP Nexus

SNPshotrs786202756
SNPdbers786202756
MSV3drs786202756
GWAS Ctlgrs786202756
Max Magnitude0
ClinVar
Risk rs786202756(;)
Alt rs786202756(;)
Reference rs786202756(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.32907470delC
CLNSRC
CLNACC RCV000165730.1,