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rs63751705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751705(G;T)
Make rs63751705(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028923
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751705
ebirs63751705
HLIrs63751705
Exacrs63751705
Varsomers63751705
Maprs63751705
PheGenIrs63751705
hapmaprs63751705
1000 genomesrs63751705
hgdprs63751705
ensemblrs63751705
gopubmedrs63751705
geneviewrs63751705
scholarrs63751705
googlers63751705
pharmgkbrs63751705
gwascentralrs63751705
openSNPrs63751705
23andMers63751705
23andMe allrs63751705
SNP Nexus

SNPshotrs63751705
SNPdbers63751705
MSV3drs63751705
GWAS Ctlgrs63751705
Max Magnitude0
ClinVar
Risk rs63751705(C,T;C,T)
Alt rs63751705(C,T;C,T)
Reference rs63751705(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070414G>C; NC_000003.11:g.37070414G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000129764.2, RCV000075239.2,