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rs786203073

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203073(-;-)
Make rs786203073(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5986891
GenePMS2
is asnp
is mentioned by
dbSNPrs786203073
ebirs786203073
HLIrs786203073
Exacrs786203073
Varsomers786203073
Maprs786203073
PheGenIrs786203073
hapmaprs786203073
1000 genomesrs786203073
hgdprs786203073
ensemblrs786203073
gopubmedrs786203073
geneviewrs786203073
scholarrs786203073
googlers786203073
pharmgkbrs786203073
gwascentralrs786203073
openSNPrs786203073
23andMers786203073
23andMe allrs786203073
SNP Nexus

SNPshotrs786203073
SNPdbers786203073
MSV3drs786203073
GWAS Ctlgrs786203073
Max Magnitude0
ClinVar
Risk rs786203073(;)
Alt rs786203073(;)
Reference rs786203073(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6026522delA
CLNSRC
CLNACC RCV000166215.1, RCV000229520.1,