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rs587778961

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778961(-;-)
Make rs587778961(-;T)
Make rs587778961(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048540
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778961
ebirs587778961
HLIrs587778961
Exacrs587778961
Varsomers587778961
Maprs587778961
PheGenIrs587778961
hapmaprs587778961
1000 genomesrs587778961
hgdprs587778961
ensemblrs587778961
gopubmedrs587778961
geneviewrs587778961
scholarrs587778961
googlers587778961
pharmgkbrs587778961
gwascentralrs587778961
openSNPrs587778961
23andMers587778961
23andMe allrs587778961
SNP Nexus

SNPshotrs587778961
SNPdbers587778961
MSV3drs587778961
GWAS Ctlgrs587778961
Max Magnitude0
ClinVar
Risk rs587778961(T;T)
Alt rs587778961(T;T)
Reference rs587778961(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090031_37090032insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075428.2,