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rs587778937

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778937(C;C)
Make rs587778937(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040291
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778937
ebirs587778937
HLIrs587778937
Exacrs587778937
Varsomers587778937
Maprs587778937
PheGenIrs587778937
hapmaprs587778937
1000 genomesrs587778937
hgdprs587778937
ensemblrs587778937
gopubmedrs587778937
geneviewrs587778937
scholarrs587778937
googlers587778937
pharmgkbrs587778937
gwascentralrs587778937
openSNPrs587778937
23andMers587778937
23andMe allrs587778937
SNP Nexus

SNPshotrs587778937
SNPdbers587778937
MSV3drs587778937
GWAS Ctlgrs587778937
Max Magnitude0
ClinVar
Risk rs587778937(C;C)
Alt rs587778937(C;C)
Reference rs587778937(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081782T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075296.2,