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rs63751592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
(AGAA;AGAA) 0 common in clinvar
Make rs63751592(-;-)
Make rs63751592(-;AAGA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028785
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751592
ebirs63751592
HLIrs63751592
Exacrs63751592
Varsomers63751592
Maprs63751592
PheGenIrs63751592
hapmaprs63751592
1000 genomesrs63751592
hgdprs63751592
ensemblrs63751592
gopubmedrs63751592
geneviewrs63751592
scholarrs63751592
googlers63751592
pharmgkbrs63751592
gwascentralrs63751592
openSNPrs63751592
23andMers63751592
23andMe allrs63751592
SNP Nexus

SNPshotrs63751592
SNPdbers63751592
MSV3drs63751592
GWAS Ctlgrs63751592
Max Magnitude0
ClinVar
Risk rs63751592(;)
Alt rs63751592(;)
Reference rs63751592(AGAA;AGAA)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37070276_37070279delAAGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075201.2, RCV000162473.1,