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rs587778957

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778957(-;-)
Make rs587778957(-;A)
Make rs587778957(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048524
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778957
ebirs587778957
HLIrs587778957
Exacrs587778957
Varsomers587778957
Maprs587778957
PheGenIrs587778957
hapmaprs587778957
1000 genomesrs587778957
hgdprs587778957
ensemblrs587778957
gopubmedrs587778957
geneviewrs587778957
scholarrs587778957
googlers587778957
pharmgkbrs587778957
gwascentralrs587778957
openSNPrs587778957
23andMers587778957
23andMe allrs587778957
SNP Nexus

SNPshotrs587778957
SNPdbers587778957
MSV3drs587778957
GWAS Ctlgrs587778957
Max Magnitude0
ClinVar
Risk rs587778957(A;A)
Alt rs587778957(A;A)
Reference rs587778957(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090015dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075417.2,