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rs587778979

From SNPedia

Orientationplus
Geno Mag Summary
(GTGAAGTGCC;GTGAAGTGCC) 0 common in clinvar
Make rs587778979(-;-)
Make rs587778979(-;GTGAAGTGCC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050487
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778979
ebirs587778979
HLIrs587778979
Exacrs587778979
Varsomers587778979
Maprs587778979
PheGenIrs587778979
hapmaprs587778979
1000 genomesrs587778979
hgdprs587778979
ensemblrs587778979
gopubmedrs587778979
geneviewrs587778979
scholarrs587778979
googlers587778979
pharmgkbrs587778979
gwascentralrs587778979
openSNPrs587778979
23andMers587778979
23andMe allrs587778979
SNP Nexus

SNPshotrs587778979
SNPdbers587778979
MSV3drs587778979
GWAS Ctlgrs587778979
Max Magnitude0
ClinVar
Risk rs587778979(;)
Alt rs587778979(;)
Reference rs587778979(GTGAAGTGCC;GTGAAGTGCC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37091978_37091987delGTGAAGTGCC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075545.2,