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rs587778971

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778971(G;T)
Make rs587778971(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048949
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778971
ebirs587778971
HLIrs587778971
Exacrs587778971
Varsomers587778971
Maprs587778971
PheGenIrs587778971
hapmaprs587778971
1000 genomesrs587778971
hgdprs587778971
ensemblrs587778971
gopubmedrs587778971
geneviewrs587778971
scholarrs587778971
googlers587778971
pharmgkbrs587778971
gwascentralrs587778971
openSNPrs587778971
23andMers587778971
23andMe allrs587778971
SNP Nexus

SNPshotrs587778971
SNPdbers587778971
MSV3drs587778971
GWAS Ctlgrs587778971
Max Magnitude0
ClinVar
Risk rs587778971(T;T)
Alt rs587778971(T;T)
Reference rs587778971(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090440G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075489.2,