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rs863225378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs863225378(ATCTGGACC;ATCTGGACC)
Make rs863225378(ATCTGGACC;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37047577
GeneMLH1
is asnp
is mentioned by
dbSNPrs863225378
ClinGenrs863225378
ebirs863225378
HLIrs863225378
Exacrs863225378
Varsomers863225378
Maprs863225378
PheGenIrs863225378
hapmaprs863225378
1000 genomesrs863225378
hgdprs863225378
ensemblrs863225378
gopubmedrs863225378
geneviewrs863225378
scholarrs863225378
googlers863225378
pharmgkbrs863225378
gwascentralrs863225378
openSNPrs863225378
23andMers863225378
23andMe allrs863225378
SNP Nexus

SNPshotrs863225378
SNPdbers863225378
MSV3drs863225378
GWAS Ctlgrs863225378
Max Magnitude0
ClinVar
Risk rs863225378(ATCTGGACC;ATCTGGACC)
Alt rs863225378(ATCTGGACC;ATCTGGACC)
Reference Rs863225378(GG;GG)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MLH1
CLNDBN not provided Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089068_37089069delGGinsATCTGGACC
CLNSRC
CLNACC RCV000202288.1, RCV000218337.1, RCV000475245.1,