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rs587779035

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779035(A;G)
Make rs587779035(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37014430
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779035
ebirs587779035
HLIrs587779035
Exacrs587779035
Varsomers587779035
Maprs587779035
PheGenIrs587779035
hapmaprs587779035
1000 genomesrs587779035
hgdprs587779035
ensemblrs587779035
gopubmedrs587779035
geneviewrs587779035
scholarrs587779035
googlers587779035
pharmgkbrs587779035
gwascentralrs587779035
openSNPrs587779035
23andMers587779035
23andMe allrs587779035
SNP Nexus

SNPshotrs587779035
SNPdbers587779035
MSV3drs587779035
GWAS Ctlgrs587779035
Max Magnitude0
ClinVar
Risk rs587779035(G;G)
Alt rs587779035(G;G)
Reference rs587779035(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055921A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075815.2,