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rs587778949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778949(A;TTCTT)
Make rs587778949(TTCTT;TTCTT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047640
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778949
ClinGenrs587778949
ebirs587778949
HLIrs587778949
Exacrs587778949
Varsomers587778949
Maprs587778949
PheGenIrs587778949
hapmaprs587778949
1000 genomesrs587778949
hgdprs587778949
ensemblrs587778949
gopubmedrs587778949
geneviewrs587778949
scholarrs587778949
googlers587778949
pharmgkbrs587778949
gwascentralrs587778949
openSNPrs587778949
23andMers587778949
23andMe allrs587778949
SNP Nexus

SNPshotrs587778949
SNPdbers587778949
MSV3drs587778949
GWAS Ctlgrs587778949
Max Magnitude0
ClinVar
Risk rs587778949(TTCTT;TTCTT)
Alt rs587778949(TTCTT;TTCTT)
Reference Rs587778949(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089131delAinsTTCTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075386.2,