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rs587779012

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779012(-;-)
Make rs587779012(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37006999
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779012
ebirs587779012
HLIrs587779012
Exacrs587779012
Varsomers587779012
Maprs587779012
PheGenIrs587779012
hapmaprs587779012
1000 genomesrs587779012
hgdprs587779012
ensemblrs587779012
gopubmedrs587779012
geneviewrs587779012
scholarrs587779012
googlers587779012
pharmgkbrs587779012
gwascentralrs587779012
openSNPrs587779012
23andMers587779012
23andMe allrs587779012
SNP Nexus

SNPshotrs587779012
SNPdbers587779012
MSV3drs587779012
GWAS Ctlgrs587779012
Max Magnitude0
ClinVar
Risk rs587779012(;)
Alt rs587779012(;)
Reference rs587779012(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048490delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075694.2,