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rs587778919

From SNPedia

Orientationplus
Geno Mag Summary
(GAAAG;GAAAG) 0 common in clinvar
Make rs587778919(-;-)
Make rs587778919(-;GGAAA)
Make rs587778919(GGAAA;GGAAA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028838
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778919
ebirs587778919
HLIrs587778919
Exacrs587778919
Varsomers587778919
Maprs587778919
PheGenIrs587778919
hapmaprs587778919
1000 genomesrs587778919
hgdprs587778919
ensemblrs587778919
gopubmedrs587778919
geneviewrs587778919
scholarrs587778919
googlers587778919
pharmgkbrs587778919
gwascentralrs587778919
openSNPrs587778919
23andMers587778919
23andMe allrs587778919
SNP Nexus

SNPshotrs587778919
SNPdbers587778919
MSV3drs587778919
GWAS Ctlgrs587778919
Max Magnitude0
ClinVar
Risk rs587778919(;)
Alt rs587778919(;)
Reference rs587778919(GAAAG;GAAAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070329_37070333delGGAAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075222.2,