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rs863224829

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTA;AGTA) 0 common in clinvar
Make rs863224829(-;-)
Make rs863224829(-;AGTA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799593
GeneMSH6
is asnp
is mentioned by
dbSNPrs863224829
dbSNP (old)rs863224829
ClinGenrs863224829
ebirs863224829
HLIrs863224829
Exacrs863224829
Gnomadrs863224829
Varsomers863224829
Maprs863224829
PheGenIrs863224829
Biobankrs863224829
1000 genomesrs863224829
hgdprs863224829
ensemblrs863224829
gopubmedrs863224829
geneviewrs863224829
scholarrs863224829
googlers863224829
pharmgkbrs863224829
gwascentralrs863224829
openSNPrs863224829
23andMers863224829
23andMe allrs863224829
SNP Nexus

SNPshotrs863224829
SNPdbers863224829
MSV3drs863224829
GWAS Ctlgrs863224829
Max Magnitude0
ClinVar
Risk rs863224829(-;-)
Alt rs863224829(-;-)
Reference Rs863224829(AGTA;AGTA)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026732_48026735delAGTA
CLNSRC
CLNACC RCV000196707.1, RCV000213843.2,