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rs63751266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751266(-;-)
Make rs63751266(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996663
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751266
ebirs63751266
HLIrs63751266
Exacrs63751266
Varsomers63751266
Maprs63751266
PheGenIrs63751266
hapmaprs63751266
1000 genomesrs63751266
hgdprs63751266
ensemblrs63751266
gopubmedrs63751266
geneviewrs63751266
scholarrs63751266
googlers63751266
pharmgkbrs63751266
gwascentralrs63751266
openSNPrs63751266
23andMers63751266
23andMe allrs63751266
SNP Nexus

SNPshotrs63751266
SNPdbers63751266
MSV3drs63751266
GWAS Ctlgrs63751266
Max Magnitude0
ClinVar
Risk rs63751266(;)
Alt rs63751266(;)
Reference rs63751266(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038154delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075280.2,