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rs587778975

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778975(C;G)
Make rs587778975(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37049007
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778975
ebirs587778975
HLIrs587778975
Exacrs587778975
Varsomers587778975
Maprs587778975
PheGenIrs587778975
hapmaprs587778975
1000 genomesrs587778975
hgdprs587778975
ensemblrs587778975
gopubmedrs587778975
geneviewrs587778975
scholarrs587778975
googlers587778975
pharmgkbrs587778975
gwascentralrs587778975
openSNPrs587778975
23andMers587778975
23andMe allrs587778975
SNP Nexus

SNPshotrs587778975
SNPdbers587778975
MSV3drs587778975
GWAS Ctlgrs587778975
Max Magnitude0
ClinVar
Risk rs587778975(G;G)
Alt rs587778975(G;G)
Reference rs587778975(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090498C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075525.2,