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rs587779041

From SNPedia

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Geno Mag Summary
(GTTTAGATC;GTTTAGATC) 0 common in clinvar
Make rs587779041(-;-)
Make rs587779041(-;TTAGATCGT)
Make rs587779041(TTAGATCGT;TTAGATCGT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017502
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779041
ebirs587779041
HLIrs587779041
Exacrs587779041
Varsomers587779041
Maprs587779041
PheGenIrs587779041
hapmaprs587779041
1000 genomesrs587779041
hgdprs587779041
ensemblrs587779041
gopubmedrs587779041
geneviewrs587779041
scholarrs587779041
googlers587779041
pharmgkbrs587779041
gwascentralrs587779041
openSNPrs587779041
23andMers587779041
23andMe allrs587779041
SNP Nexus

SNPshotrs587779041
SNPdbers587779041
MSV3drs587779041
GWAS Ctlgrs587779041
Max Magnitude0
ClinVar
Risk rs587779041(;)
Alt rs587779041(;)
Reference rs587779041(GTTTAGATC;GTTTAGATC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37058993_37059001delTTAGATCGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075864.2,