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rs863224450

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224450(A;A)
Make rs863224450(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position6002452
GenePMS2
is asnp
is mentioned by
dbSNPrs863224450
ebirs863224450
HLIrs863224450
Exacrs863224450
Varsomers863224450
Maprs863224450
PheGenIrs863224450
hapmaprs863224450
1000 genomesrs863224450
hgdprs863224450
ensemblrs863224450
gopubmedrs863224450
geneviewrs863224450
scholarrs863224450
googlers863224450
pharmgkbrs863224450
gwascentralrs863224450
openSNPrs863224450
23andMers863224450
23andMe allrs863224450
SNP Nexus

SNPshotrs863224450
SNPdbers863224450
MSV3drs863224450
GWAS Ctlgrs863224450
Max Magnitude0
ClinVar
Risk rs863224450(A;A)
Alt rs863224450(A;A)
Reference rs863224450(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6042083C>T
CLNSRC
CLNACC RCV000200046.2,