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rs63751428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751428(C;T)
Make rs63751428(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996686
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751428
ebirs63751428
HLIrs63751428
Exacrs63751428
Varsomers63751428
Maprs63751428
PheGenIrs63751428
hapmaprs63751428
1000 genomesrs63751428
hgdprs63751428
ensemblrs63751428
gopubmedrs63751428
geneviewrs63751428
scholarrs63751428
googlers63751428
pharmgkbrs63751428
gwascentralrs63751428
openSNPrs63751428
23andMers63751428
23andMe allrs63751428
SNP Nexus

SNPshotrs63751428
SNPdbers63751428
MSV3drs63751428
GWAS Ctlgrs63751428
Max Magnitude0
ClinVar
Risk rs63751428(A,T;A,T)
Alt rs63751428(A,T;A,T)
Reference rs63751428(C;C)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37038177C>A; NC_000003.11:g.37038177C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075378.2, RCV000075379.2, RCV000217644.1,