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rs587778997

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778997(-;-)
Make rs587778997(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37000979
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778997
ebirs587778997
HLIrs587778997
Exacrs587778997
Varsomers587778997
Maprs587778997
PheGenIrs587778997
hapmaprs587778997
1000 genomesrs587778997
hgdprs587778997
ensemblrs587778997
gopubmedrs587778997
geneviewrs587778997
scholarrs587778997
googlers587778997
pharmgkbrs587778997
gwascentralrs587778997
openSNPrs587778997
23andMers587778997
23andMe allrs587778997
SNP Nexus

SNPshotrs587778997
SNPdbers587778997
MSV3drs587778997
GWAS Ctlgrs587778997
Max Magnitude0
ClinVar
Risk rs587778997(;)
Alt rs587778997(;)
Reference rs587778997(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042470delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075600.2,