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rs587778929

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778929(A;A)
Make rs587778929(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040201
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778929
ebirs587778929
HLIrs587778929
Exacrs587778929
Varsomers587778929
Maprs587778929
PheGenIrs587778929
hapmaprs587778929
1000 genomesrs587778929
hgdprs587778929
ensemblrs587778929
gopubmedrs587778929
geneviewrs587778929
scholarrs587778929
googlers587778929
pharmgkbrs587778929
gwascentralrs587778929
openSNPrs587778929
23andMers587778929
23andMe allrs587778929
SNP Nexus

SNPshotrs587778929
SNPdbers587778929
MSV3drs587778929
GWAS Ctlgrs587778929
Max Magnitude0
ClinVar
Risk rs587778929(A;A)
Alt rs587778929(A;A)
Reference rs587778929(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081692T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075271.2,