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rs587779046

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779046(-;-)
Make rs587779046(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017575
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779046
ebirs587779046
HLIrs587779046
Exacrs587779046
Varsomers587779046
Maprs587779046
PheGenIrs587779046
hapmaprs587779046
1000 genomesrs587779046
hgdprs587779046
ensemblrs587779046
gopubmedrs587779046
geneviewrs587779046
scholarrs587779046
googlers587779046
pharmgkbrs587779046
gwascentralrs587779046
openSNPrs587779046
23andMers587779046
23andMe allrs587779046
SNP Nexus

SNPshotrs587779046
SNPdbers587779046
MSV3drs587779046
GWAS Ctlgrs587779046
Max Magnitude0
ClinVar
Risk rs587779046(;)
Alt rs587779046(;)
Reference rs587779046(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059066delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075891.2,