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rs863225386

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225386(A;T)
Make rs863225386(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47429842
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225386
ebirs863225386
HLIrs863225386
Exacrs863225386
Varsomers863225386
Maprs863225386
PheGenIrs863225386
hapmaprs863225386
1000 genomesrs863225386
hgdprs863225386
ensemblrs863225386
gopubmedrs863225386
geneviewrs863225386
scholarrs863225386
googlers863225386
pharmgkbrs863225386
gwascentralrs863225386
openSNPrs863225386
23andMers863225386
23andMe allrs863225386
SNP Nexus

SNPshotrs863225386
SNPdbers863225386
MSV3drs863225386
GWAS Ctlgrs863225386
Max Magnitude0
ClinVar
Risk rs863225386(C,T;C,T)
Alt rs863225386(C,T;C,T)
Reference rs863225386(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47656981A>C; NC_000002.11:g.47656981A>T
CLNSRC
CLNACC RCV000231260.1, RCV000202154.1,