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rs587778953

From SNPedia

Orientationplus
Geno Mag Summary
(TCTT;TCTT) 0 common in clinvar
Make rs587778953(-;-)
Make rs587778953(-;CTTT)
Make rs587778953(CTTT;CTTT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047667
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778953
ebirs587778953
HLIrs587778953
Exacrs587778953
Varsomers587778953
Maprs587778953
PheGenIrs587778953
hapmaprs587778953
1000 genomesrs587778953
hgdprs587778953
ensemblrs587778953
gopubmedrs587778953
geneviewrs587778953
scholarrs587778953
googlers587778953
pharmgkbrs587778953
gwascentralrs587778953
openSNPrs587778953
23andMers587778953
23andMe allrs587778953
SNP Nexus

SNPshotrs587778953
SNPdbers587778953
MSV3drs587778953
GWAS Ctlgrs587778953
Max Magnitude0
ClinVar
Risk rs587778953(;)
Alt rs587778953(;)
Reference rs587778953(TCTT;TCTT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089158_37089161delCTTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075400.2,