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rs63751710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs63751710(AG;GTT)
Make rs63751710(GTT;GTT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37006995
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751710
ebirs63751710
HLIrs63751710
Exacrs63751710
Varsomers63751710
Maprs63751710
PheGenIrs63751710
hapmaprs63751710
1000 genomesrs63751710
hgdprs63751710
ensemblrs63751710
gopubmedrs63751710
geneviewrs63751710
scholarrs63751710
googlers63751710
pharmgkbrs63751710
gwascentralrs63751710
openSNPrs63751710
23andMers63751710
23andMe allrs63751710
SNP Nexus

SNPshotrs63751710
SNPdbers63751710
MSV3drs63751710
GWAS Ctlgrs63751710
Max Magnitude0
ClinVar
Risk rs63751710(GTT;GTT)
Alt rs63751710(GTT;GTT)
Reference rs63751710(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048486_37048487delAGinsGTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075690.2,