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rs786202875

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202875(G;T)
Make rs786202875(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32336849
GeneBRCA2
is asnp
is mentioned by
dbSNPrs786202875
ebirs786202875
HLIrs786202875
Exacrs786202875
Varsomers786202875
Maprs786202875
PheGenIrs786202875
hapmaprs786202875
1000 genomesrs786202875
hgdprs786202875
ensemblrs786202875
gopubmedrs786202875
geneviewrs786202875
scholarrs786202875
googlers786202875
pharmgkbrs786202875
gwascentralrs786202875
openSNPrs786202875
23andMers786202875
23andMe allrs786202875
SNP Nexus

SNPshotrs786202875
SNPdbers786202875
MSV3drs786202875
GWAS Ctlgrs786202875
Max Magnitude0
ClinVar
Risk rs786202875(T;T)
Alt rs786202875(T;T)
Reference rs786202875(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.32910986G>T
CLNSRC
CLNACC RCV000165924.1,