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rs63751415

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751415(G;G)
Make rs63751415(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047662
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751415
ebirs63751415
HLIrs63751415
Exacrs63751415
Varsomers63751415
Maprs63751415
PheGenIrs63751415
hapmaprs63751415
1000 genomesrs63751415
hgdprs63751415
ensemblrs63751415
gopubmedrs63751415
geneviewrs63751415
scholarrs63751415
googlers63751415
pharmgkbrs63751415
gwascentralrs63751415
openSNPrs63751415
23andMers63751415
23andMe allrs63751415
SNP Nexus

SNPshotrs63751415
SNPdbers63751415
MSV3drs63751415
GWAS Ctlgrs63751415
Max Magnitude0
ClinVar
Risk rs63751415(G;G)
Alt rs63751415(G;G)
Reference rs63751415(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089153T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075393.2,