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rs864622261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAT;AAT) 0 common in clinvar
Make rs864622261(AAT;TG)
Make rs864622261(TG;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47414295
GeneMSH2
is asnp
is mentioned by
dbSNPrs864622261
ClinGenrs864622261
ebirs864622261
HLIrs864622261
Exacrs864622261
Varsomers864622261
Maprs864622261
PheGenIrs864622261
hapmaprs864622261
1000 genomesrs864622261
hgdprs864622261
ensemblrs864622261
gopubmedrs864622261
geneviewrs864622261
scholarrs864622261
googlers864622261
pharmgkbrs864622261
gwascentralrs864622261
openSNPrs864622261
23andMers864622261
23andMe allrs864622261
SNP Nexus

SNPshotrs864622261
SNPdbers864622261
MSV3drs864622261
GWAS Ctlgrs864622261
Max Magnitude0
ClinVar
Risk rs864622261(TG;TG)
Alt rs864622261(TG;TG)
Reference Rs864622261(AAT;AAT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641434_47641436delAATinsTG
CLNSRC
CLNACC RCV000205875.1,