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rs573125799

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs573125799(A;A)
Make rs573125799(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5997364
GenePMS2
is asnp
is mentioned by
dbSNPrs573125799
ebirs573125799
HLIrs573125799
Exacrs573125799
Varsomers573125799
Maprs573125799
PheGenIrs573125799
hapmaprs573125799
1000 genomesrs573125799
hgdprs573125799
ensemblrs573125799
gopubmedrs573125799
geneviewrs573125799
scholarrs573125799
googlers573125799
pharmgkbrs573125799
gwascentralrs573125799
openSNPrs573125799
23andMers573125799
23andMe allrs573125799
SNP Nexus

SNPshotrs573125799
SNPdbers573125799
MSV3drs573125799
GWAS Ctlgrs573125799
Max Magnitude0
ClinVar
Risk rs573125799(A,T;A,T)
Alt rs573125799(A,T;A,T)
Reference rs573125799(G;G)
Significance Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene PMS2
CLNDBN not specified Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000007.13:g.6036995G>A; NC_000007.13:g.6036995G>T
CLNSRC
CLNACC RCV000127457.2, RCV000162412.1, RCV000168447.4,