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rs587779058

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779058(C;T)
Make rs587779058(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37020407
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779058
ebirs587779058
HLIrs587779058
Exacrs587779058
Varsomers587779058
Maprs587779058
PheGenIrs587779058
hapmaprs587779058
1000 genomesrs587779058
hgdprs587779058
ensemblrs587779058
gopubmedrs587779058
geneviewrs587779058
scholarrs587779058
googlers587779058
pharmgkbrs587779058
gwascentralrs587779058
openSNPrs587779058
23andMers587779058
23andMe allrs587779058
SNP Nexus

SNPshotrs587779058
SNPdbers587779058
MSV3drs587779058
GWAS Ctlgrs587779058
Max Magnitude0
ClinVar
Risk rs587779058(T;T)
Alt rs587779058(T;T)
Reference rs587779058(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37061898C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075952.2, RCV000166394.1,