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rs863225393

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225393(-;TA)
Make rs863225393(TA;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47478356
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225393
ClinGenrs863225393
ebirs863225393
HLIrs863225393
Exacrs863225393
Varsomers863225393
Maprs863225393
PheGenIrs863225393
hapmaprs863225393
1000 genomesrs863225393
hgdprs863225393
ensemblrs863225393
gopubmedrs863225393
geneviewrs863225393
scholarrs863225393
googlers863225393
pharmgkbrs863225393
gwascentralrs863225393
openSNPrs863225393
23andMers863225393
23andMe allrs863225393
SNP Nexus

SNPshotrs863225393
SNPdbers863225393
MSV3drs863225393
GWAS Ctlgrs863225393
Max Magnitude0
ClinVar
Risk rs863225393(TA;TA)
Alt rs863225393(TA;TA)
Reference Rs863225393(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47705495_47705496insTA
CLNSRC
CLNACC RCV000202054.1,