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rs63751302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751302(C;T)
Make rs63751302(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37007055
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751302
ebirs63751302
HLIrs63751302
Exacrs63751302
Varsomers63751302
Maprs63751302
PheGenIrs63751302
hapmaprs63751302
1000 genomesrs63751302
hgdprs63751302
ensemblrs63751302
gopubmedrs63751302
geneviewrs63751302
scholarrs63751302
googlers63751302
pharmgkbrs63751302
gwascentralrs63751302
openSNPrs63751302
23andMers63751302
23andMe allrs63751302
SNP Nexus

SNPshotrs63751302
SNPdbers63751302
MSV3drs63751302
GWAS Ctlgrs63751302
Max Magnitude0
ClinVar
Risk rs63751302(T;T)
Alt rs63751302(T;T)
Reference rs63751302(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048546C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075708.2,