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rs863224496

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224496(A;T)
Make rs863224496(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5987468
GenePMS2
is asnp
is mentioned by
dbSNPrs863224496
ebirs863224496
HLIrs863224496
Exacrs863224496
Varsomers863224496
Maprs863224496
PheGenIrs863224496
hapmaprs863224496
1000 genomesrs863224496
hgdprs863224496
ensemblrs863224496
gopubmedrs863224496
geneviewrs863224496
scholarrs863224496
googlers863224496
pharmgkbrs863224496
gwascentralrs863224496
openSNPrs863224496
23andMers863224496
23andMe allrs863224496
SNP Nexus

SNPshotrs863224496
SNPdbers863224496
MSV3drs863224496
GWAS Ctlgrs863224496
Max Magnitude0
ClinVar
Risk rs863224496(T;T)
Alt rs863224496(T;T)
Reference rs863224496(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6027099T>A
CLNSRC
CLNACC RCV000198386.1,