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rs587778912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGAGACATCGGG;AAGAGACATCGGG) 0 common in clinvar
Make rs587778912(-;-)
Make rs587778912(-;GACATCGGGAAGA)
Make rs587778912(GACATCGGGAAGA;GACATCGGGAAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028789
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778912
dbSNP (old)rs587778912
ClinGenrs587778912
ebirs587778912
HLIrs587778912
Exacrs587778912
Gnomadrs587778912
Varsomers587778912
Maprs587778912
PheGenIrs587778912
Biobankrs587778912
1000 genomesrs587778912
hgdprs587778912
ensemblrs587778912
gopubmedrs587778912
geneviewrs587778912
scholarrs587778912
googlers587778912
pharmgkbrs587778912
gwascentralrs587778912
openSNPrs587778912
23andMers587778912
23andMe allrs587778912
SNP Nexus

SNPshotrs587778912
SNPdbers587778912
MSV3drs587778912
GWAS Ctlgrs587778912
Max Magnitude0
ClinVar
Risk rs587778912(-;-)
Alt rs587778912(-;-)
Reference Rs587778912(AAGAGACATCGGG;AAGAGACATCGGG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070280_37070292delGACATCGGGAAGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075208.2,