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rs587778954

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778954(-;-)
Make rs587778954(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047680
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778954
ebirs587778954
HLIrs587778954
Exacrs587778954
Varsomers587778954
Maprs587778954
PheGenIrs587778954
hapmaprs587778954
1000 genomesrs587778954
hgdprs587778954
ensemblrs587778954
gopubmedrs587778954
geneviewrs587778954
scholarrs587778954
googlers587778954
pharmgkbrs587778954
gwascentralrs587778954
openSNPrs587778954
23andMers587778954
23andMe allrs587778954
SNP Nexus

SNPshotrs587778954
SNPdbers587778954
MSV3drs587778954
GWAS Ctlgrs587778954
Max Magnitude0
ClinVar
Risk rs587778954(;)
Alt rs587778954(;)
Reference rs587778954(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089171delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075403.2,