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rs63751616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751616(C;C)
Make rs63751616(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047532
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751616
ebirs63751616
HLIrs63751616
Exacrs63751616
Varsomers63751616
Maprs63751616
PheGenIrs63751616
hapmaprs63751616
1000 genomesrs63751616
hgdprs63751616
ensemblrs63751616
gopubmedrs63751616
geneviewrs63751616
scholarrs63751616
googlers63751616
pharmgkbrs63751616
gwascentralrs63751616
openSNPrs63751616
23andMers63751616
23andMe allrs63751616
SNP Nexus

SNPshotrs63751616
SNPdbers63751616
MSV3drs63751616
GWAS Ctlgrs63751616
Max Magnitude0
ClinVar
Risk rs63751616(C;C)
Alt rs63751616(C;C)
Reference rs63751616(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089023T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075347.2,