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rs267608173

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGAA;AGAA) 0 common in clinvar
Make rs267608173(-;-)
Make rs267608173(-;AGAA)
ReferenceGRCh38 38.1/141
Chromosome7
Position5978625
GenePMS2
is asnp
is mentioned by
dbSNPrs267608173
ebirs267608173
HLIrs267608173
Exacrs267608173
Varsomers267608173
Maprs267608173
PheGenIrs267608173
hapmaprs267608173
1000 genomesrs267608173
hgdprs267608173
ensemblrs267608173
gopubmedrs267608173
geneviewrs267608173
scholarrs267608173
googlers267608173
pharmgkbrs267608173
gwascentralrs267608173
openSNPrs267608173
23andMers267608173
23andMe allrs267608173
SNP Nexus

SNPshotrs267608173
SNPdbers267608173
MSV3drs267608173
GWAS Ctlgrs267608173
Max Magnitude0
ClinVar
Risk rs267608173(;)
Alt rs267608173(;)
Reference rs267608173(AGAA;AGAA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6018256_6018259delTTCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076848.2,