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rs63751310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751310(C;T)
Make rs63751310(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048595
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751310
ebirs63751310
HLIrs63751310
Exacrs63751310
Varsomers63751310
Maprs63751310
PheGenIrs63751310
hapmaprs63751310
1000 genomesrs63751310
hgdprs63751310
ensemblrs63751310
gopubmedrs63751310
geneviewrs63751310
scholarrs63751310
googlers63751310
pharmgkbrs63751310
gwascentralrs63751310
openSNPrs63751310
23andMers63751310
23andMe allrs63751310
SNP Nexus

SNPshotrs63751310
SNPdbers63751310
MSV3drs63751310
GWAS Ctlgrs63751310
Max Magnitude0
ClinVar
Risk rs63751310(T;T)
Alt rs63751310(T;T)
Reference rs63751310(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37090086C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075444.2, RCV000128869.2, RCV000202252.1,