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rs863224481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGAGGACGCGCTGC;CGAGGACGCGCTGC) 0 common in clinvar
Make rs863224481(-;-)
Make rs863224481(-;CGAGGACGCGCTGC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47403332
GeneMSH2
is asnp
is mentioned by
dbSNPrs863224481
ClinGenrs863224481
ebirs863224481
HLIrs863224481
Exacrs863224481
Varsomers863224481
Maprs863224481
PheGenIrs863224481
hapmaprs863224481
1000 genomesrs863224481
hgdprs863224481
ensemblrs863224481
gopubmedrs863224481
geneviewrs863224481
scholarrs863224481
googlers863224481
pharmgkbrs863224481
gwascentralrs863224481
openSNPrs863224481
23andMers863224481
23andMe allrs863224481
SNP Nexus

SNPshotrs863224481
SNPdbers863224481
MSV3drs863224481
GWAS Ctlgrs863224481
Max Magnitude0
ClinVar
Risk rs863224481(-;-)
Alt rs863224481(-;-)
Reference Rs863224481(CGAGGACGCGCTGC;CGAGGACGCGCTGC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630471_47630484delCGAGGACGCGCTGC
CLNSRC
CLNACC RCV000199618.2,