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rs63751255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751255(-;-)
Make rs63751255(-;A)
Make rs63751255(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996693
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751255
ebirs63751255
HLIrs63751255
Exacrs63751255
Varsomers63751255
Maprs63751255
PheGenIrs63751255
hapmaprs63751255
1000 genomesrs63751255
hgdprs63751255
ensemblrs63751255
gopubmedrs63751255
geneviewrs63751255
scholarrs63751255
googlers63751255
pharmgkbrs63751255
gwascentralrs63751255
openSNPrs63751255
23andMers63751255
23andMe allrs63751255
SNP Nexus

SNPshotrs63751255
SNPdbers63751255
MSV3drs63751255
GWAS Ctlgrs63751255
Max Magnitude0
ClinVar
Risk rs63751255(A;A)
Alt rs63751255(A;A)
Reference rs63751255(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038184dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075427.2,