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rs587778998

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778998(A;G)
Make rs587778998(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37000991
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778998
ebirs587778998
HLIrs587778998
Exacrs587778998
Varsomers587778998
Maprs587778998
PheGenIrs587778998
hapmaprs587778998
1000 genomesrs587778998
hgdprs587778998
ensemblrs587778998
gopubmedrs587778998
geneviewrs587778998
scholarrs587778998
googlers587778998
pharmgkbrs587778998
gwascentralrs587778998
openSNPrs587778998
23andMers587778998
23andMe allrs587778998
SNP Nexus

SNPshotrs587778998
SNPdbers587778998
MSV3drs587778998
GWAS Ctlgrs587778998
Max Magnitude0
ClinVar
Risk rs587778998(G;G)
Alt rs587778998(G;G)
Reference rs587778998(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37042482A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075602.3, RCV000166056.1,