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rs786202790

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202790(-;-)
Make rs786202790(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47475058
GeneMSH2
is asnp
is mentioned by
dbSNPrs786202790
ebirs786202790
HLIrs786202790
Exacrs786202790
Varsomers786202790
Maprs786202790
PheGenIrs786202790
hapmaprs786202790
1000 genomesrs786202790
hgdprs786202790
ensemblrs786202790
gopubmedrs786202790
geneviewrs786202790
scholarrs786202790
googlers786202790
pharmgkbrs786202790
gwascentralrs786202790
openSNPrs786202790
23andMers786202790
23andMe allrs786202790
SNP Nexus

SNPshotrs786202790
SNPdbers786202790
MSV3drs786202790
GWAS Ctlgrs786202790
Max Magnitude0
ClinVar
Risk rs786202790(;)
Alt rs786202790(;)
Reference rs786202790(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47702197delT
CLNSRC
CLNACC RCV000165778.1,