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rs587778938

From SNPedia

Orientationplus
Geno Mag Summary
(TAAATCA;TAAATCA) 0 common in clinvar
Make rs587778938(ATTT;ATTT)
Make rs587778938(ATTT;TAAATCA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040296
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778938
ebirs587778938
HLIrs587778938
Exacrs587778938
Varsomers587778938
Maprs587778938
PheGenIrs587778938
hapmaprs587778938
1000 genomesrs587778938
hgdprs587778938
ensemblrs587778938
gopubmedrs587778938
geneviewrs587778938
scholarrs587778938
googlers587778938
pharmgkbrs587778938
gwascentralrs587778938
openSNPrs587778938
23andMers587778938
23andMe allrs587778938
SNP Nexus

SNPshotrs587778938
SNPdbers587778938
MSV3drs587778938
GWAS Ctlgrs587778938
Max Magnitude0
ClinVar
Risk rs587778938(ATTT;ATTT)
Alt rs587778938(ATTT;ATTT)
Reference rs587778938(TAAATCA;TAAATCA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081787_37081793delTAAATCAinsATTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075298.2,