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rs786203456

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203456(-;-)
Make rs786203456(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37047645
GeneMLH1
is asnp
is mentioned by
dbSNPrs786203456
ebirs786203456
HLIrs786203456
Exacrs786203456
Varsomers786203456
Maprs786203456
PheGenIrs786203456
hapmaprs786203456
1000 genomesrs786203456
hgdprs786203456
ensemblrs786203456
gopubmedrs786203456
geneviewrs786203456
scholarrs786203456
googlers786203456
pharmgkbrs786203456
gwascentralrs786203456
openSNPrs786203456
23andMers786203456
23andMe allrs786203456
SNP Nexus

SNPshotrs786203456
SNPdbers786203456
MSV3drs786203456
GWAS Ctlgrs786203456
Max Magnitude0
ClinVar
Risk rs786203456(;)
Alt rs786203456(;)
Reference rs786203456(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37089136delG
CLNSRC
CLNACC RCV000166770.1,