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rs587779015

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779015(-;-)
Make rs587779015(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37007030
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779015
ebirs587779015
HLIrs587779015
Exacrs587779015
Varsomers587779015
Maprs587779015
PheGenIrs587779015
hapmaprs587779015
1000 genomesrs587779015
hgdprs587779015
ensemblrs587779015
gopubmedrs587779015
geneviewrs587779015
scholarrs587779015
googlers587779015
pharmgkbrs587779015
gwascentralrs587779015
openSNPrs587779015
23andMers587779015
23andMe allrs587779015
SNP Nexus

SNPshotrs587779015
SNPdbers587779015
MSV3drs587779015
GWAS Ctlgrs587779015
Max Magnitude0
ClinVar
Risk rs587779015(;)
Alt rs587779015(;)
Reference rs587779015(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048521delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075703.2,