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rs267607744

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607744(A;A)
Make rs267607744(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37006990
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607744
ebirs267607744
HLIrs267607744
Exacrs267607744
Varsomers267607744
Maprs267607744
PheGenIrs267607744
hapmaprs267607744
1000 genomesrs267607744
hgdprs267607744
ensemblrs267607744
gopubmedrs267607744
geneviewrs267607744
scholarrs267607744
googlers267607744
pharmgkbrs267607744
gwascentralrs267607744
openSNPrs267607744
23andMers267607744
23andMe allrs267607744
SNP Nexus

SNPshotrs267607744
SNPdbers267607744
MSV3drs267607744
GWAS Ctlgrs267607744
Max Magnitude0
ClinVar
Risk rs267607744(A;A)
Alt rs267607744(A;A)
Reference rs267607744(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048481G>A
CLNSRC
CLNACC RCV000205947.2,