Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs63751651(-;-)
Make rs63751651(-;AG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050486
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751651
ebirs63751651
HLIrs63751651
Exacrs63751651
Varsomers63751651
Maprs63751651
PheGenIrs63751651
hapmaprs63751651
1000 genomesrs63751651
hgdprs63751651
ensemblrs63751651
gopubmedrs63751651
geneviewrs63751651
scholarrs63751651
googlers63751651
pharmgkbrs63751651
gwascentralrs63751651
openSNPrs63751651
23andMers63751651
23andMe allrs63751651
SNP Nexus

SNPshotrs63751651
SNPdbers63751651
MSV3drs63751651
GWAS Ctlgrs63751651
Max Magnitude0
ClinVar
Risk rs63751651(;)
Alt rs63751651(;)
Reference rs63751651(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37091977_37091978delAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075544.2,