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rs63751607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751607(-;-)
Make rs63751607(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37004472
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751607
ebirs63751607
HLIrs63751607
Exacrs63751607
Varsomers63751607
Maprs63751607
PheGenIrs63751607
hapmaprs63751607
1000 genomesrs63751607
hgdprs63751607
ensemblrs63751607
gopubmedrs63751607
geneviewrs63751607
scholarrs63751607
googlers63751607
pharmgkbrs63751607
gwascentralrs63751607
openSNPrs63751607
23andMers63751607
23andMe allrs63751607
SNP Nexus

SNPshotrs63751607
SNPdbers63751607
MSV3drs63751607
GWAS Ctlgrs63751607
Max Magnitude0
ClinVar
Risk rs63751607(;)
Alt rs63751607(;)
Reference rs63751607(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045963delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075675.2,