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rs267607900

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607900(A;T)
Make rs267607900(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37050645
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607900
ebirs267607900
HLIrs267607900
Exacrs267607900
Varsomers267607900
Maprs267607900
PheGenIrs267607900
hapmaprs267607900
1000 genomesrs267607900
hgdprs267607900
ensemblrs267607900
gopubmedrs267607900
geneviewrs267607900
scholarrs267607900
googlers267607900
pharmgkbrs267607900
gwascentralrs267607900
openSNPrs267607900
23andMers267607900
23andMe allrs267607900
SNP Nexus

SNPshotrs267607900
SNPdbers267607900
MSV3drs267607900
GWAS Ctlgrs267607900
Max Magnitude0
ClinVar
Risk rs267607900(T;T)
Alt rs267607900(T;T)
Reference rs267607900(A;A)
Significance Pathogenic
Disease Lynch syndrome I Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome I Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092136A>G; NC_000003.11:g.37092136A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000206724.1, RCV000075591.2,