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

rs863225416

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225416(-;AATT)
Make rs863225416(AATT;AATT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806516
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs863225416
dbSNP (old)rs863225416
ClinGenrs863225416
ebirs863225416
HLIrs863225416
Exacrs863225416
Varsomers863225416
Maprs863225416
PheGenIrs863225416
Biobankrs863225416
1000 genomesrs863225416
hgdprs863225416
ensemblrs863225416
gopubmedrs863225416
geneviewrs863225416
scholarrs863225416
googlers863225416
pharmgkbrs863225416
gwascentralrs863225416
openSNPrs863225416
23andMers863225416
23andMe allrs863225416
SNP Nexus

SNPshotrs863225416
SNPdbers863225416
MSV3drs863225416
GWAS Ctlgrs863225416
Max Magnitude0
ClinVar
Risk rs863225416(AATT;AATT)
Alt rs863225416(AATT;AATT)
Reference Rs863225416(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FBXO11 MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033652_48033655dupAATT
CLNSRC
CLNACC RCV000202223.1,