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rs63751200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(D;D) 0
(GA;GA) 0 common in clinvar
Make rs63751200(-;-)
Make rs63751200(-;GA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048596
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751200
ebirs63751200
HLIrs63751200
Exacrs63751200
Varsomers63751200
Maprs63751200
PheGenIrs63751200
hapmaprs63751200
1000 genomesrs63751200
hgdprs63751200
ensemblrs63751200
gopubmedrs63751200
geneviewrs63751200
scholarrs63751200
googlers63751200
pharmgkbrs63751200
gwascentralrs63751200
openSNPrs63751200
23andMers63751200
23andMe allrs63751200
SNP Nexus

SNPshotrs63751200
SNPdbers63751200
MSV3drs63751200
GWAS Ctlgrs63751200
Max Magnitude0
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,