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rs587778981

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587778981(-;-)
Make rs587778981(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050529
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778981
ebirs587778981
HLIrs587778981
Exacrs587778981
Varsomers587778981
Maprs587778981
PheGenIrs587778981
hapmaprs587778981
1000 genomesrs587778981
hgdprs587778981
ensemblrs587778981
gopubmedrs587778981
geneviewrs587778981
scholarrs587778981
googlers587778981
pharmgkbrs587778981
gwascentralrs587778981
openSNPrs587778981
23andMers587778981
23andMe allrs587778981
SNP Nexus

SNPshotrs587778981
SNPdbers587778981
MSV3drs587778981
GWAS Ctlgrs587778981
Max Magnitude0
ClinVar
Risk rs587778981(;)
Alt rs587778981(;)
Reference rs587778981(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092020_37092021delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075555.2,