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rs797045117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045117(-;-)
Make rs797045117(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position75047540
GeneMLH3
is asnp
is mentioned by
dbSNPrs797045117
dbSNP (classic)rs797045117
ClinGenrs797045117
ebirs797045117
HLIrs797045117
Exacrs797045117
Gnomadrs797045117
Varsomers797045117
LitVarrs797045117
Maprs797045117
PheGenIrs797045117
Biobankrs797045117
1000 genomesrs797045117
hgdprs797045117
ensemblrs797045117
geneviewrs797045117
scholarrs797045117
googlers797045117
pharmgkbrs797045117
gwascentralrs797045117
openSNPrs797045117
23andMers797045117
SNPshotrs797045117
SNPdbers797045117
MSV3drs797045117
GWAS Ctlgrs797045117
Max Magnitude0
ClinVar
Risk rs797045117(-;-)
Alt rs797045117(-;-)
Reference Rs797045117(A;A)
Significance Probable-Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 7
Variation info
Gene MLH3
CLNDBN Hereditary nonpolyposis colorectal cancer type 7
Reversed 1
HGVS NC_000014.8:g.75514243delT
CLNSRC
CLNACC RCV000190646.1,