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rs587778923

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs587778923(-;-)
Make rs587778923(-;AAGA)
Make rs587778923(AAGA;AAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996657
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778923
ebirs587778923
HLIrs587778923
Exacrs587778923
Varsomers587778923
Maprs587778923
PheGenIrs587778923
hapmaprs587778923
1000 genomesrs587778923
hgdprs587778923
ensemblrs587778923
gopubmedrs587778923
geneviewrs587778923
scholarrs587778923
googlers587778923
pharmgkbrs587778923
gwascentralrs587778923
openSNPrs587778923
23andMers587778923
23andMe allrs587778923
SNP Nexus

SNPshotrs587778923
SNPdbers587778923
MSV3drs587778923
GWAS Ctlgrs587778923
Max Magnitude0
ClinVar
Risk rs587778923(;)
Alt rs587778923(;)
Reference rs587778923(AAAG;AAAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038148_37038151delAAGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075264.2,