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

rs786201990

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201990(-;-)
Make rs786201990(-;T)
Make rs786201990(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37047677
GeneMLH1
is asnp
is mentioned by
dbSNPrs786201990
ebirs786201990
HLIrs786201990
Exacrs786201990
Varsomers786201990
Maprs786201990
PheGenIrs786201990
hapmaprs786201990
1000 genomesrs786201990
hgdprs786201990
ensemblrs786201990
gopubmedrs786201990
geneviewrs786201990
scholarrs786201990
googlers786201990
pharmgkbrs786201990
gwascentralrs786201990
openSNPrs786201990
23andMers786201990
23andMe allrs786201990
SNP Nexus

SNPshotrs786201990
SNPdbers786201990
MSV3drs786201990
GWAS Ctlgrs786201990
Max Magnitude0
ClinVar
Risk rs786201990(T;T)
Alt rs786201990(T;T)
Reference rs786201990(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37089168dupT
CLNSRC
CLNACC RCV000164560.1,