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rs63751200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GA) 6 Lynch syndrome, pathogenic mutation
(D;D) 0
(GA;GA) 0 common in clinvar


Make rs63751200(-;-)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048596
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751200
dbSNP (classic)rs63751200
ClinGenrs63751200
ebirs63751200
HLIrs63751200
Exacrs63751200
Gnomadrs63751200
Varsomers63751200
LitVarrs63751200
Maprs63751200
PheGenIrs63751200
Biobankrs63751200
1000 genomesrs63751200
hgdprs63751200
ensemblrs63751200
geneviewrs63751200
scholarrs63751200
googlers63751200
pharmgkbrs63751200
gwascentralrs63751200
openSNPrs63751200
23andMers63751200
SNPshotrs63751200
SNPdbers63751200
MSV3drs63751200
GWAS Ctlgrs63751200
Max Magnitude6
ClinVar
Risk rs63751200(-;-)
Alt rs63751200(-;-)
Reference Rs63751200(GA;GA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090087_37090088delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075449.2,