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rs786203036

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203036(G;G)
Make rs786203036(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47463086
GeneMSH2
is asnp
is mentioned by
dbSNPrs786203036
ebirs786203036
HLIrs786203036
Exacrs786203036
Varsomers786203036
Maprs786203036
PheGenIrs786203036
hapmaprs786203036
1000 genomesrs786203036
hgdprs786203036
ensemblrs786203036
gopubmedrs786203036
geneviewrs786203036
scholarrs786203036
googlers786203036
pharmgkbrs786203036
gwascentralrs786203036
openSNPrs786203036
23andMers786203036
23andMe allrs786203036
SNP Nexus

SNPshotrs786203036
SNPdbers786203036
MSV3drs786203036
GWAS Ctlgrs786203036
Max Magnitude0
ClinVar
Risk rs786203036(A,G;A,G)
Alt rs786203036(A,G;A,G)
Reference rs786203036(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47690225T>A; NC_000002.11:g.47690225T>G
CLNSRC
CLNACC RCV000168254.1, RCV000166169.1,