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rs267607893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607893(C;G)
Make rs267607893(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37050632
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607893
dbSNP (old)rs267607893
ClinGenrs267607893
ebirs267607893
HLIrs267607893
Exacrs267607893
Gnomadrs267607893
Varsomers267607893
Maprs267607893
PheGenIrs267607893
Biobankrs267607893
1000 genomesrs267607893
hgdprs267607893
ensemblrs267607893
gopubmedrs267607893
geneviewrs267607893
scholarrs267607893
googlers267607893
pharmgkbrs267607893
gwascentralrs267607893
openSNPrs267607893
23andMers267607893
23andMe allrs267607893
SNPshotrs267607893
SNPdbers267607893
MSV3drs267607893
GWAS Ctlgrs267607893
Max Magnitude0
ClinVar
Risk rs267607893(A;A) rs267607893(G;G) rs267607893(T;T)
Alt rs267607893(A;A) rs267607893(G;G) rs267607893(T;T)
Reference Rs267607893(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37092123C>A; NC_000003.11:g.37092123C>G
CLNSRC
CLNACC RCV000075584.2, RCV000075585.2, RCV000482247.1,