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rs587778883

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778883(-;-)
Make rs587778883(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025648
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778883
ebirs587778883
HLIrs587778883
Exacrs587778883
Varsomers587778883
Maprs587778883
PheGenIrs587778883
hapmaprs587778883
1000 genomesrs587778883
hgdprs587778883
ensemblrs587778883
gopubmedrs587778883
geneviewrs587778883
scholarrs587778883
googlers587778883
pharmgkbrs587778883
gwascentralrs587778883
openSNPrs587778883
23andMers587778883
23andMe allrs587778883
SNP Nexus

SNPshotrs587778883
SNPdbers587778883
MSV3drs587778883
GWAS Ctlgrs587778883
Max Magnitude0
ClinVar
Risk rs587778883(;)
Alt rs587778883(;)
Reference rs587778883(A;A)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37067139delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075103.2, RCV000115450.3,