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rs63751632

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751632(A;A)
Make rs63751632(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047683
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751632
ClinGenrs63751632
ebirs63751632
HLIrs63751632
Exacrs63751632
Varsomers63751632
Maprs63751632
PheGenIrs63751632
hapmaprs63751632
1000 genomesrs63751632
hgdprs63751632
ensemblrs63751632
gopubmedrs63751632
geneviewrs63751632
scholarrs63751632
googlers63751632
pharmgkbrs63751632
gwascentralrs63751632
openSNPrs63751632
23andMers63751632
23andMe allrs63751632
SNP Nexus

SNPshotrs63751632
SNPdbers63751632
MSV3drs63751632
GWAS Ctlgrs63751632
Max Magnitude0
ClinVar
Risk rs63751632(A;A)
Alt rs63751632(A;A)
Reference Rs63751632(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089174G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075409.2,