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

rs863225398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAT;GAT) 0 common in clinvar
Make rs863225398(AA;AA)
Make rs863225398(AA;GAT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799151
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225398
dbSNP (old)rs863225398
ClinGenrs863225398
ebirs863225398
HLIrs863225398
Exacrs863225398
Gnomadrs863225398
Varsomers863225398
Maprs863225398
PheGenIrs863225398
Biobankrs863225398
1000 genomesrs863225398
hgdprs863225398
ensemblrs863225398
gopubmedrs863225398
geneviewrs863225398
scholarrs863225398
googlers863225398
pharmgkbrs863225398
gwascentralrs863225398
openSNPrs863225398
23andMers863225398
23andMe allrs863225398
SNP Nexus

SNPshotrs863225398
SNPdbers863225398
MSV3drs863225398
GWAS Ctlgrs863225398
Max Magnitude0
ClinVar
Risk rs863225398(AA;AA)
Alt rs863225398(AA;AA)
Reference Rs863225398(GAT;GAT)
Significance Other
Disease not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026290_48026292delGATinsAA
CLNSRC
CLNACC RCV000202004.1, RCV000474246.1, RCV000491518.1,