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rs863225383

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225383(A;T)
Make rs863225383(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37011857
GeneMLH1
is asnp
is mentioned by
dbSNPrs863225383
ebirs863225383
HLIrs863225383
Exacrs863225383
Varsomers863225383
Maprs863225383
PheGenIrs863225383
hapmaprs863225383
1000 genomesrs863225383
hgdprs863225383
ensemblrs863225383
gopubmedrs863225383
geneviewrs863225383
scholarrs863225383
googlers863225383
pharmgkbrs863225383
gwascentralrs863225383
openSNPrs863225383
23andMers863225383
23andMe allrs863225383
SNP Nexus

SNPshotrs863225383
SNPdbers863225383
MSV3drs863225383
GWAS Ctlgrs863225383
Max Magnitude0
ClinVar
Risk rs863225383(T;T)
Alt rs863225383(T;T)
Reference rs863225383(A;A)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37053348A>T
CLNSRC
CLNACC RCV000202144.1, RCV000216838.1,