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rs786202796

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202796(G;T)
Make rs786202796(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32332277
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202796
ebirs786202796
HLIrs786202796
Exacrs786202796
Varsomers786202796
Maprs786202796
PheGenIrs786202796
hapmaprs786202796
1000 genomesrs786202796
hgdprs786202796
ensemblrs786202796
gopubmedrs786202796
geneviewrs786202796
scholarrs786202796
googlers786202796
pharmgkbrs786202796
gwascentralrs786202796
openSNPrs786202796
23andMers786202796
23andMe allrs786202796
SNP Nexus

SNPshotrs786202796
SNPdbers786202796
MSV3drs786202796
GWAS Ctlgrs786202796
Max Magnitude0
ClinVar
Risk rs786202796(T;T)
Alt rs786202796(T;T)
Reference rs786202796(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32906414G>T
CLNSRC
CLNACC RCV000165786.1, RCV000220294.1,