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rs587778918

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778918(A;T)
Make rs587778918(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028836
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778918
ebirs587778918
HLIrs587778918
Exacrs587778918
Varsomers587778918
Maprs587778918
PheGenIrs587778918
hapmaprs587778918
1000 genomesrs587778918
hgdprs587778918
ensemblrs587778918
gopubmedrs587778918
geneviewrs587778918
scholarrs587778918
googlers587778918
pharmgkbrs587778918
gwascentralrs587778918
openSNPrs587778918
23andMers587778918
23andMe allrs587778918
SNP Nexus

SNPshotrs587778918
SNPdbers587778918
MSV3drs587778918
GWAS Ctlgrs587778918
Max Magnitude0
ClinVar
Risk rs587778918(T;T)
Alt rs587778918(T;T)
Reference rs587778918(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070327A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075220.2,