Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779055

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779055(-;-)
Make rs587779055(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37020353
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779055
ebirs587779055
HLIrs587779055
Exacrs587779055
Varsomers587779055
Maprs587779055
PheGenIrs587779055
hapmaprs587779055
1000 genomesrs587779055
hgdprs587779055
ensemblrs587779055
gopubmedrs587779055
geneviewrs587779055
scholarrs587779055
googlers587779055
pharmgkbrs587779055
gwascentralrs587779055
openSNPrs587779055
23andMers587779055
23andMe allrs587779055
SNP Nexus

SNPshotrs587779055
SNPdbers587779055
MSV3drs587779055
GWAS Ctlgrs587779055
Max Magnitude0
ClinVar
Risk rs587779055(;)
Alt rs587779055(;)
Reference rs587779055(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061844delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075939.2,