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rs587778931

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs587778931(-;-)
Make rs587778931(-;TG)
Make rs587778931(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040219
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778931
ebirs587778931
HLIrs587778931
Exacrs587778931
Varsomers587778931
Maprs587778931
PheGenIrs587778931
hapmaprs587778931
1000 genomesrs587778931
hgdprs587778931
ensemblrs587778931
gopubmedrs587778931
geneviewrs587778931
scholarrs587778931
googlers587778931
pharmgkbrs587778931
gwascentralrs587778931
openSNPrs587778931
23andMers587778931
23andMe allrs587778931
SNP Nexus

SNPshotrs587778931
SNPdbers587778931
MSV3drs587778931
GWAS Ctlgrs587778931
Max Magnitude0
ClinVar
Risk rs587778931(;)
Alt rs587778931(;)
Reference rs587778931(GT;GT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081710_37081711delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075273.2,