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rs863225388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TATACAGGCTCTGGAAAA;TATACAGGCTCTGGAAAA) 0 common in clinvar
Make rs863225388(AGTT;AGTT)
Make rs863225388(AGTT;TATACAGGCTCTGGAAAA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47429916
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225388
dbSNP (old)rs863225388
ClinGenrs863225388
ebirs863225388
HLIrs863225388
Exacrs863225388
Gnomadrs863225388
Varsomers863225388
Maprs863225388
PheGenIrs863225388
Biobankrs863225388
1000 genomesrs863225388
hgdprs863225388
ensemblrs863225388
gopubmedrs863225388
geneviewrs863225388
scholarrs863225388
googlers863225388
pharmgkbrs863225388
gwascentralrs863225388
openSNPrs863225388
23andMers863225388
23andMe allrs863225388
SNP Nexus

SNPshotrs863225388
SNPdbers863225388
MSV3drs863225388
GWAS Ctlgrs863225388
Max Magnitude0
ClinVar
Risk rs863225388(AGTT;AGTT)
Alt rs863225388(AGTT;AGTT)
Reference Rs863225388(TATACAGGCTCTGGAAAA;TATACAGGCTCTGGAAAA)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47657055_47657072del18insAGTT
CLNSRC
CLNACC RCV000202139.1, RCV000491837.1,