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rs587779037

From SNPedia

Orientationplus
Geno Mag Summary
(GTTA;GTTA) 0 common in clinvar
Make rs587779037(-;-)
Make rs587779037(-;GTTA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37014485
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779037
ebirs587779037
HLIrs587779037
Exacrs587779037
Varsomers587779037
Maprs587779037
PheGenIrs587779037
hapmaprs587779037
1000 genomesrs587779037
hgdprs587779037
ensemblrs587779037
gopubmedrs587779037
geneviewrs587779037
scholarrs587779037
googlers587779037
pharmgkbrs587779037
gwascentralrs587779037
openSNPrs587779037
23andMers587779037
23andMe allrs587779037
SNP Nexus

SNPshotrs587779037
SNPdbers587779037
MSV3drs587779037
GWAS Ctlgrs587779037
Max Magnitude0
ClinVar
Risk rs587779037(;)
Alt rs587779037(;)
Reference rs587779037(GTTA;GTTA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055976_37055979delGTTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075832.2,