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rs63749986

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749986(-;-)
Make rs63749986(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047642
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749986
ebirs63749986
HLIrs63749986
Exacrs63749986
Varsomers63749986
Maprs63749986
PheGenIrs63749986
hapmaprs63749986
1000 genomesrs63749986
hgdprs63749986
ensemblrs63749986
gopubmedrs63749986
geneviewrs63749986
scholarrs63749986
googlers63749986
pharmgkbrs63749986
gwascentralrs63749986
openSNPrs63749986
23andMers63749986
23andMe allrs63749986
SNP Nexus

SNPshotrs63749986
SNPdbers63749986
MSV3drs63749986
GWAS Ctlgrs63749986
Max Magnitude0
ClinVar
Risk rs63749986(;)
Alt rs63749986(;)
Reference rs63749986(G;G)
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.37089133delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075388.2, RCV000217973.1,