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rs587779029

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779029(A;A)
Make rs587779029(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36993552
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs587779029
ebirs587779029
HLIrs587779029
Exacrs587779029
Varsomers587779029
Maprs587779029
PheGenIrs587779029
hapmaprs587779029
1000 genomesrs587779029
hgdprs587779029
ensemblrs587779029
gopubmedrs587779029
geneviewrs587779029
scholarrs587779029
googlers587779029
pharmgkbrs587779029
gwascentralrs587779029
openSNPrs587779029
23andMers587779029
23andMe allrs587779029
SNP Nexus

SNPshotrs587779029
SNPdbers587779029
MSV3drs587779029
GWAS Ctlgrs587779029
Max Magnitude0
ClinVar
Risk rs587779029(A,T;A,T)
Alt rs587779029(A,T;A,T)
Reference rs587779029(C;C)
Significance Pathogenic
Disease Lynch syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37035043C>A; NC_000003.11:g.37035043C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075784.2, RCV000160548.1, RCV000221241.1,