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rs863224482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs863224482(-;-)
Make rs863224482(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47410146
GeneMSH2
is asnp
is mentioned by
dbSNPrs863224482
dbSNP (old)rs863224482
ClinGenrs863224482
ebirs863224482
HLIrs863224482
Exacrs863224482
Gnomadrs863224482
Varsomers863224482
Maprs863224482
PheGenIrs863224482
Biobankrs863224482
1000 genomesrs863224482
hgdprs863224482
ensemblrs863224482
gopubmedrs863224482
geneviewrs863224482
scholarrs863224482
googlers863224482
pharmgkbrs863224482
gwascentralrs863224482
openSNPrs863224482
23andMers863224482
23andMe allrs863224482
SNP Nexus

SNPshotrs863224482
SNPdbers863224482
MSV3drs863224482
GWAS Ctlgrs863224482
Merged fromRs864622556
Max Magnitude0
ClinVar
Risk rs863224482(-;-)
Alt rs863224482(-;-)
Reference Rs863224482(AT;AT)
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.47637287_47637288delAT
CLNSRC
CLNACC RCV000205179.2, RCV000491597.1,