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rs63751435

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63751435(-;-)
Make rs63751435(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028865
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751435
ebirs63751435
HLIrs63751435
Exacrs63751435
Varsomers63751435
Maprs63751435
PheGenIrs63751435
hapmaprs63751435
1000 genomesrs63751435
hgdprs63751435
ensemblrs63751435
gopubmedrs63751435
geneviewrs63751435
scholarrs63751435
googlers63751435
pharmgkbrs63751435
gwascentralrs63751435
openSNPrs63751435
23andMers63751435
23andMe allrs63751435
SNP Nexus

SNPshotrs63751435
SNPdbers63751435
MSV3drs63751435
GWAS Ctlgrs63751435
Max Magnitude0
ClinVar
Risk rs63751435(;)
Alt rs63751435(;)
Reference rs63751435(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070356delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075228.2,