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rs587779048

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779048(-;-)
Make rs587779048(-;AC)
Make rs587779048(AC;AC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017582
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779048
ebirs587779048
HLIrs587779048
Exacrs587779048
Varsomers587779048
Maprs587779048
PheGenIrs587779048
hapmaprs587779048
1000 genomesrs587779048
hgdprs587779048
ensemblrs587779048
gopubmedrs587779048
geneviewrs587779048
scholarrs587779048
googlers587779048
pharmgkbrs587779048
gwascentralrs587779048
openSNPrs587779048
23andMers587779048
23andMe allrs587779048
SNP Nexus

SNPshotrs587779048
SNPdbers587779048
MSV3drs587779048
GWAS Ctlgrs587779048
Max Magnitude0
ClinVar
Risk rs587779048(AC;AC)
Alt rs587779048(AC;AC)
Reference rs587779048(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059072_37059073dupAC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075895.2,