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rs587778932

From SNPedia

Orientationplus
Geno Mag Summary
(GAGG;GAGG) 0 common in clinvar
Make rs587778932(-;-)
Make rs587778932(-;GAGG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996663
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778932
ebirs587778932
HLIrs587778932
Exacrs587778932
Varsomers587778932
Maprs587778932
PheGenIrs587778932
hapmaprs587778932
1000 genomesrs587778932
hgdprs587778932
ensemblrs587778932
gopubmedrs587778932
geneviewrs587778932
scholarrs587778932
googlers587778932
pharmgkbrs587778932
gwascentralrs587778932
openSNPrs587778932
23andMers587778932
23andMe allrs587778932
SNP Nexus

SNPshotrs587778932
SNPdbers587778932
MSV3drs587778932
GWAS Ctlgrs587778932
Max Magnitude0
ClinVar
Risk rs587778932(;)
Alt rs587778932(;)
Reference rs587778932(GAGG;GAGG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038154_37038157delGAGG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075279.2,