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rs587778906

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778906(-;-)
Make rs587778906(-;G)
Make rs587778906(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025946
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778906
ebirs587778906
HLIrs587778906
Exacrs587778906
Varsomers587778906
Maprs587778906
PheGenIrs587778906
hapmaprs587778906
1000 genomesrs587778906
hgdprs587778906
ensemblrs587778906
gopubmedrs587778906
geneviewrs587778906
scholarrs587778906
googlers587778906
pharmgkbrs587778906
gwascentralrs587778906
openSNPrs587778906
23andMers587778906
23andMe allrs587778906
SNP Nexus

SNPshotrs587778906
SNPdbers587778906
MSV3drs587778906
GWAS Ctlgrs587778906
Max Magnitude0
ClinVar
Risk rs587778906(G;G)
Alt rs587778906(G;G)
Reference rs587778906(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067437dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075177.2,