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rs878854035

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854035(-;-)
Make rs878854035(-;C)
Make rs878854035(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5987264
GenePMS2
is asnp
is mentioned by
dbSNPrs878854035
ebirs878854035
HLIrs878854035
Exacrs878854035
Varsomers878854035
Maprs878854035
PheGenIrs878854035
hapmaprs878854035
1000 genomesrs878854035
hgdprs878854035
ensemblrs878854035
gopubmedrs878854035
geneviewrs878854035
scholarrs878854035
googlers878854035
pharmgkbrs878854035
gwascentralrs878854035
openSNPrs878854035
23andMers878854035
23andMe allrs878854035
SNP Nexus

SNPshotrs878854035
SNPdbers878854035
MSV3drs878854035
GWAS Ctlgrs878854035
Max Magnitude0
ClinVar
Risk rs878854035(C;C)
Alt rs878854035(C;C)
Reference rs878854035(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6026896dupG
CLNSRC
CLNACC RCV000230207.1,