Have questions? Visit https://www.reddit.com/r/SNPedia

rs587778896

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778896(-;-)
Make rs587778896(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996621
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778896
ebirs587778896
HLIrs587778896
Exacrs587778896
Varsomers587778896
Maprs587778896
PheGenIrs587778896
hapmaprs587778896
1000 genomesrs587778896
hgdprs587778896
ensemblrs587778896
gopubmedrs587778896
geneviewrs587778896
scholarrs587778896
googlers587778896
pharmgkbrs587778896
gwascentralrs587778896
openSNPrs587778896
23andMers587778896
23andMe allrs587778896
SNP Nexus

SNPshotrs587778896
SNPdbers587778896
MSV3drs587778896
GWAS Ctlgrs587778896
Max Magnitude0
ClinVar
Risk rs587778896(;)
Alt rs587778896(;)
Reference rs587778896(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038112delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075148.2,