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rs587779032

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs587779032(AT;AT)
Make rs587779032(AT;GG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37012099
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779032
ebirs587779032
HLIrs587779032
Exacrs587779032
Varsomers587779032
Maprs587779032
PheGenIrs587779032
hapmaprs587779032
1000 genomesrs587779032
hgdprs587779032
ensemblrs587779032
gopubmedrs587779032
geneviewrs587779032
scholarrs587779032
googlers587779032
pharmgkbrs587779032
gwascentralrs587779032
openSNPrs587779032
23andMers587779032
23andMe allrs587779032
SNP Nexus

SNPshotrs587779032
SNPdbers587779032
MSV3drs587779032
GWAS Ctlgrs587779032
Max Magnitude0
ClinVar
Risk rs587779032(AT;AT)
Alt rs587779032(AT;AT)
Reference rs587779032(GG;GG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053590_37053591delGGinsAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075811.2,