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rs267607771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 Lynch syndrome, pathogenic mutation
Make rs267607771(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37014549
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607771
dbSNP (old)rs267607771
ClinGenrs267607771
ebirs267607771
HLIrs267607771
Exacrs267607771
Gnomadrs267607771
Varsomers267607771
LitVarrs267607771
Maprs267607771
PheGenIrs267607771
Biobankrs267607771
1000 genomesrs267607771
hgdprs267607771
ensemblrs267607771
gopubmedrs267607771
geneviewrs267607771
scholarrs267607771
googlers267607771
pharmgkbrs267607771
gwascentralrs267607771
openSNPrs267607771
23andMers267607771
23andMe allrs267607771
SNPshotrs267607771
SNPdbers267607771
MSV3drs267607771
GWAS Ctlgrs267607771
Max Magnitude6
ClinVar
Risk rs267607771(T;T)
Alt rs267607771(T;T)
Reference Rs267607771(G;G)
Significance Pathogenic
Disease Lynch syndrome I
Variation info
Gene MLH1
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000003.11:g.37056040G>T
CLNSRC
CLNACC RCV000075855.2,