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rs63751652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGCA;AGCA) 0 common in clinvar
(I;I) 0
Make rs63751652(-;-)
Make rs63751652(-;AGCA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37049013
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751652
ebirs63751652
HLIrs63751652
Exacrs63751652
Varsomers63751652
Maprs63751652
PheGenIrs63751652
hapmaprs63751652
1000 genomesrs63751652
hgdprs63751652
ensemblrs63751652
gopubmedrs63751652
geneviewrs63751652
scholarrs63751652
googlers63751652
pharmgkbrs63751652
gwascentralrs63751652
openSNPrs63751652
23andMers63751652
23andMe allrs63751652
SNP Nexus

SNPshotrs63751652
SNPdbers63751652
MSV3drs63751652
GWAS Ctlgrs63751652
Max Magnitude0
ClinVar
Risk rs63751652(;)
Alt rs63751652(;)
Reference rs63751652(AGCA;AGCA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090504_37090507delAGCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075526.2,