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rs587778921

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778921(-;-)
Make rs587778921(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028894
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778921
ebirs587778921
HLIrs587778921
Exacrs587778921
Varsomers587778921
Maprs587778921
PheGenIrs587778921
hapmaprs587778921
1000 genomesrs587778921
hgdprs587778921
ensemblrs587778921
gopubmedrs587778921
geneviewrs587778921
scholarrs587778921
googlers587778921
pharmgkbrs587778921
gwascentralrs587778921
openSNPrs587778921
23andMers587778921
23andMe allrs587778921
SNP Nexus

SNPshotrs587778921
SNPdbers587778921
MSV3drs587778921
GWAS Ctlgrs587778921
Max Magnitude0
ClinVar
Risk rs587778921(;)
Alt rs587778921(;)
Reference rs587778921(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070385delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075232.2,