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rs587778968

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778968(-;-)
Make rs587778968(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996703
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778968
ebirs587778968
HLIrs587778968
Exacrs587778968
Varsomers587778968
Maprs587778968
PheGenIrs587778968
hapmaprs587778968
1000 genomesrs587778968
hgdprs587778968
ensemblrs587778968
gopubmedrs587778968
geneviewrs587778968
scholarrs587778968
googlers587778968
pharmgkbrs587778968
gwascentralrs587778968
openSNPrs587778968
23andMers587778968
23andMe allrs587778968
SNP Nexus

SNPshotrs587778968
SNPdbers587778968
MSV3drs587778968
GWAS Ctlgrs587778968
Max Magnitude0
ClinVar
Risk rs587778968(;)
Alt rs587778968(;)
Reference rs587778968(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038194delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075484.2,