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rs267608150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCCCCT;CCCCCT) 0 common in clinvar
Make rs267608150(CCCCCT;TGTGTGTGAAG)
Make rs267608150(TGTGTGTGAAG;TGTGTGTGAAG)
ReferenceGRCh38 38.1/141
Chromosome7
Position5997388
GenePMS2
is asnp
is mentioned by
dbSNPrs267608150
ebirs267608150
HLIrs267608150
Exacrs267608150
Varsomers267608150
Maprs267608150
PheGenIrs267608150
hapmaprs267608150
1000 genomesrs267608150
hgdprs267608150
ensemblrs267608150
gopubmedrs267608150
geneviewrs267608150
scholarrs267608150
googlers267608150
pharmgkbrs267608150
gwascentralrs267608150
openSNPrs267608150
23andMers267608150
23andMe allrs267608150
SNP Nexus

SNPshotrs267608150
SNPdbers267608150
MSV3drs267608150
GWAS Ctlgrs267608150
Max Magnitude0
ClinVar
Risk rs267608150(TGTGTGTGAAG;TGTGTGTGAAG)
Alt rs267608150(TGTGTGTGAAG;TGTGTGTGAAG)
Reference rs267608150(CCCCCT;CCCCCT)
Significance Pathogenic
Disease Lynch syndrome Neoplastic Syndromes
Variation info
Gene PMS2
CLNDBN Lynch syndrome Neoplastic Syndromes, Hereditary
Reversed 1
HGVS NC_000007.14:g.5997388_5997393delAGGGGGinsCTTCACACACA
CLNSRC ClinVar GeneDx InSiGHT
CLNACC RCV000076885.1, RCV000115703.1,