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rs587778964

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778964(A;C)
Make rs587778964(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048604
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778964
ebirs587778964
HLIrs587778964
Exacrs587778964
Varsomers587778964
Maprs587778964
PheGenIrs587778964
hapmaprs587778964
1000 genomesrs587778964
hgdprs587778964
ensemblrs587778964
gopubmedrs587778964
geneviewrs587778964
scholarrs587778964
googlers587778964
pharmgkbrs587778964
gwascentralrs587778964
openSNPrs587778964
23andMers587778964
23andMe allrs587778964
SNP Nexus

SNPshotrs587778964
SNPdbers587778964
MSV3drs587778964
GWAS Ctlgrs587778964
Max Magnitude0
ClinVar
Risk rs587778964(C;C)
Alt rs587778964(C;C)
Reference rs587778964(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090095A>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075450.2,