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rs587778956

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778956(-;-)
Make rs587778956(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048522
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778956
ebirs587778956
HLIrs587778956
Exacrs587778956
Varsomers587778956
Maprs587778956
PheGenIrs587778956
hapmaprs587778956
1000 genomesrs587778956
hgdprs587778956
ensemblrs587778956
gopubmedrs587778956
geneviewrs587778956
scholarrs587778956
googlers587778956
pharmgkbrs587778956
gwascentralrs587778956
openSNPrs587778956
23andMers587778956
23andMe allrs587778956
SNP Nexus

SNPshotrs587778956
SNPdbers587778956
MSV3drs587778956
GWAS Ctlgrs587778956
Max Magnitude0
ClinVar
Risk rs587778956(;)
Alt rs587778956(;)
Reference rs587778956(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090013delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075415.2,