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rs754716792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs754716792(-;-)
Make rs754716792(-;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position75046862
GeneMLH3
is asnp
is mentioned by
dbSNPrs754716792
dbSNP (classic)rs754716792
ClinGenrs754716792
ebirs754716792
HLIrs754716792
Exacrs754716792
Gnomadrs754716792
Varsomers754716792
LitVarrs754716792
Maprs754716792
PheGenIrs754716792
Biobankrs754716792
1000 genomesrs754716792
hgdprs754716792
ensemblrs754716792
geneviewrs754716792
scholarrs754716792
googlers754716792
pharmgkbrs754716792
gwascentralrs754716792
openSNPrs754716792
23andMers754716792
SNPshotrs754716792
SNPdbers754716792
MSV3drs754716792
GWAS Ctlgrs754716792
Max Magnitude0
ClinVar
Risk rs754716792(-;-)
Alt rs754716792(-;-)
Reference Rs754716792(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH3
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.75513565_75513566delTC
CLNSRC
CLNACC RCV000486748.1,