Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779027

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779027(G;T)
Make rs587779027(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37012010
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779027
ebirs587779027
HLIrs587779027
Exacrs587779027
Varsomers587779027
Maprs587779027
PheGenIrs587779027
hapmaprs587779027
1000 genomesrs587779027
hgdprs587779027
ensemblrs587779027
gopubmedrs587779027
geneviewrs587779027
scholarrs587779027
googlers587779027
pharmgkbrs587779027
gwascentralrs587779027
openSNPrs587779027
23andMers587779027
23andMe allrs587779027
SNP Nexus

SNPshotrs587779027
SNPdbers587779027
MSV3drs587779027
GWAS Ctlgrs587779027
Max Magnitude0
ClinVar
Risk rs587779027(T;T)
Alt rs587779027(T;T)
Reference rs587779027(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053501G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075779.2,