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rs863225384

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 6 Lynch syndrome
(C;C) 0 common in clinvar
(I;I) 0 common genotype


Make rs863225384(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37017508
GeneMLH1
is asnp
is mentioned by
dbSNPrs863225384
dbSNP (classic)rs863225384
ClinGenrs863225384
ebirs863225384
HLIrs863225384
Exacrs863225384
Gnomadrs863225384
Varsomers863225384
LitVarrs863225384
Maprs863225384
PheGenIrs863225384
Biobankrs863225384
1000 genomesrs863225384
hgdprs863225384
ensemblrs863225384
geneviewrs863225384
scholarrs863225384
googlers863225384
pharmgkbrs863225384
gwascentralrs863225384
openSNPrs863225384
23andMers863225384
SNPshotrs863225384
SNPdbers863225384
MSV3drs863225384
GWAS Ctlgrs863225384
Max Magnitude6
ClinVar
Risk rs863225384(-;-)
Alt rs863225384(-;-)
Reference Rs863225384(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37058999delC
CLNSRC
CLNACC RCV000202224.1,