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rs267607750

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607750(G;T)
Make rs267607750(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007064
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607750
ebirs267607750
HLIrs267607750
Exacrs267607750
Varsomers267607750
Maprs267607750
PheGenIrs267607750
hapmaprs267607750
1000 genomesrs267607750
hgdprs267607750
ensemblrs267607750
gopubmedrs267607750
geneviewrs267607750
scholarrs267607750
googlers267607750
pharmgkbrs267607750
gwascentralrs267607750
openSNPrs267607750
23andMers267607750
23andMe allrs267607750
SNP Nexus

SNPshotrs267607750
SNPdbers267607750
MSV3drs267607750
GWAS Ctlgrs267607750
Max Magnitude0
ClinVar
Risk rs267607750(T;T)
Alt rs267607750(T;T)
Reference rs267607750(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37048555G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075712.2, RCV000160522.2,