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rs863225417

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225417(-;TCAAAAGGGACATAGAAAA)
Make rs863225417(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806589
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs863225417
dbSNP (old)rs863225417
ClinGenrs863225417
ebirs863225417
HLIrs863225417
Exacrs863225417
Gnomadrs863225417
Varsomers863225417
Maprs863225417
PheGenIrs863225417
Biobankrs863225417
1000 genomesrs863225417
hgdprs863225417
ensemblrs863225417
gopubmedrs863225417
geneviewrs863225417
scholarrs863225417
googlers863225417
pharmgkbrs863225417
gwascentralrs863225417
openSNPrs863225417
23andMers863225417
23andMe allrs863225417
SNP Nexus

SNPshotrs863225417
SNPdbers863225417
MSV3drs863225417
GWAS Ctlgrs863225417
Max Magnitude0
ClinVar
Risk rs863225417(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
Alt rs863225417(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
Reference Rs863225417(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FBXO11 MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033728_48033729insTCAAAAGGGACATAGAAAA
CLNSRC
CLNACC RCV000202018.1,