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rs863224498

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs863224498(-;-)
Make rs863224498(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5987126
GenePMS2
is asnp
is mentioned by
dbSNPrs863224498
dbSNP (old)rs863224498
ClinGenrs863224498
ebirs863224498
HLIrs863224498
Exacrs863224498
Gnomadrs863224498
Varsomers863224498
Maprs863224498
PheGenIrs863224498
Biobankrs863224498
1000 genomesrs863224498
hgdprs863224498
ensemblrs863224498
gopubmedrs863224498
geneviewrs863224498
scholarrs863224498
googlers863224498
pharmgkbrs863224498
gwascentralrs863224498
openSNPrs863224498
23andMers863224498
23andMe allrs863224498
SNP Nexus

SNPshotrs863224498
SNPdbers863224498
MSV3drs863224498
GWAS Ctlgrs863224498
Max Magnitude0
ClinVar
Risk rs863224498(-;-)
Alt rs863224498(-;-)
Reference Rs863224498(TT;TT)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene PMS2
CLNDBN Lynch syndrome not provided
Reversed 1
HGVS NC_000007.13:g.6026757_6026758delAA
CLNSRC
CLNACC RCV000198235.2, RCV000479164.1,