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rs587778960

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778960(-;-)
Make rs587778960(-;T)
Make rs587778960(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048536
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778960
ebirs587778960
HLIrs587778960
Exacrs587778960
Varsomers587778960
Maprs587778960
PheGenIrs587778960
hapmaprs587778960
1000 genomesrs587778960
hgdprs587778960
ensemblrs587778960
gopubmedrs587778960
geneviewrs587778960
scholarrs587778960
googlers587778960
pharmgkbrs587778960
gwascentralrs587778960
openSNPrs587778960
23andMers587778960
23andMe allrs587778960
SNP Nexus

SNPshotrs587778960
SNPdbers587778960
MSV3drs587778960
GWAS Ctlgrs587778960
Max Magnitude0
ClinVar
Risk rs587778960(T;T)
Alt rs587778960(T;T)
Reference rs587778960(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090027dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075423.2,