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rs587779021

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779021(A;A)
Make rs587779021(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37008905
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779021
ebirs587779021
HLIrs587779021
Exacrs587779021
Varsomers587779021
Maprs587779021
PheGenIrs587779021
hapmaprs587779021
1000 genomesrs587779021
hgdprs587779021
ensemblrs587779021
gopubmedrs587779021
geneviewrs587779021
scholarrs587779021
googlers587779021
pharmgkbrs587779021
gwascentralrs587779021
openSNPrs587779021
23andMers587779021
23andMe allrs587779021
SNP Nexus

SNPshotrs587779021
SNPdbers587779021
MSV3drs587779021
GWAS Ctlgrs587779021
Max Magnitude0
ClinVar
Risk rs587779021(A,C;A,C)
Alt rs587779021(A,C;A,C)
Reference rs587779021(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050396G>A; NC_000003.11:g.37050396G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075753.2, RCV000210209.1,