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rs63751286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751286(-;-)
Make rs63751286(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012087
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751286
ebirs63751286
HLIrs63751286
Exacrs63751286
Varsomers63751286
Maprs63751286
PheGenIrs63751286
hapmaprs63751286
1000 genomesrs63751286
hgdprs63751286
ensemblrs63751286
gopubmedrs63751286
geneviewrs63751286
scholarrs63751286
googlers63751286
pharmgkbrs63751286
gwascentralrs63751286
openSNPrs63751286
23andMers63751286
23andMe allrs63751286
SNP Nexus

SNPshotrs63751286
SNPdbers63751286
MSV3drs63751286
GWAS Ctlgrs63751286
Max Magnitude0
ClinVar
Risk rs63751286(;)
Alt rs63751286(;)
Reference rs63751286(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053578delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075797.3,