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rs587778881

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778881(-;-)
Make rs587778881(-;G)
Make rs587778881(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37020451
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778881
ebirs587778881
HLIrs587778881
Exacrs587778881
Varsomers587778881
Maprs587778881
PheGenIrs587778881
hapmaprs587778881
1000 genomesrs587778881
hgdprs587778881
ensemblrs587778881
gopubmedrs587778881
geneviewrs587778881
scholarrs587778881
googlers587778881
pharmgkbrs587778881
gwascentralrs587778881
openSNPrs587778881
23andMers587778881
23andMe allrs587778881
SNP Nexus

SNPshotrs587778881
SNPdbers587778881
MSV3drs587778881
GWAS Ctlgrs587778881
Max Magnitude0
ClinVar
Risk rs587778881(G;G)
Alt rs587778881(G;G)
Reference rs587778881(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061942dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075077.2,