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rs878854037

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854037(G;T)
Make rs878854037(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5987174
GenePMS2
is asnp
is mentioned by
dbSNPrs878854037
ebirs878854037
HLIrs878854037
Exacrs878854037
Varsomers878854037
Maprs878854037
PheGenIrs878854037
hapmaprs878854037
1000 genomesrs878854037
hgdprs878854037
ensemblrs878854037
gopubmedrs878854037
geneviewrs878854037
scholarrs878854037
googlers878854037
pharmgkbrs878854037
gwascentralrs878854037
openSNPrs878854037
23andMers878854037
23andMe allrs878854037
SNP Nexus

SNPshotrs878854037
SNPdbers878854037
MSV3drs878854037
GWAS Ctlgrs878854037
Max Magnitude0
ClinVar
Risk rs878854037(T;T)
Alt rs878854037(T;T)
Reference rs878854037(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6026805C>A
CLNSRC
CLNACC RCV000234464.1,