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rs786203893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTCTAGTGGCAGGGCTA;TTCTAGTGGCAGGGCTA) 0 common in clinvar
Make rs786203893(-;-)
Make rs786203893(-;TTCTAGTGGCAGGGCTA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37025855
GeneMLH1
is asnp
is mentioned by
dbSNPrs786203893
dbSNP (old)rs786203893
ClinGenrs786203893
ebirs786203893
HLIrs786203893
Exacrs786203893
Varsomers786203893
Maprs786203893
PheGenIrs786203893
Biobankrs786203893
1000 genomesrs786203893
hgdprs786203893
ensemblrs786203893
gopubmedrs786203893
geneviewrs786203893
scholarrs786203893
googlers786203893
pharmgkbrs786203893
gwascentralrs786203893
openSNPrs786203893
23andMers786203893
23andMe allrs786203893
SNP Nexus

SNPshotrs786203893
SNPdbers786203893
MSV3drs786203893
GWAS Ctlgrs786203893
Max Magnitude0
ClinVar
Risk rs786203893(-;-)
Alt rs786203893(-;-)
Reference Rs786203893(TTCTAGTGGCAGGGCTA;TTCTAGTGGCAGGGCTA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37067346_37067362del17
CLNSRC
CLNACC RCV000167395.1,