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rs863225418

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225418(-;T)
Make rs863225418(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806649
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs863225418
ClinGenrs863225418
ebirs863225418
HLIrs863225418
Exacrs863225418
Varsomers863225418
Maprs863225418
PheGenIrs863225418
hapmaprs863225418
1000 genomesrs863225418
hgdprs863225418
ensemblrs863225418
gopubmedrs863225418
geneviewrs863225418
scholarrs863225418
googlers863225418
pharmgkbrs863225418
gwascentralrs863225418
openSNPrs863225418
23andMers863225418
23andMe allrs863225418
SNP Nexus

SNPshotrs863225418
SNPdbers863225418
MSV3drs863225418
GWAS Ctlgrs863225418
Max Magnitude0
ClinVar
Risk rs863225418(T;T)
Alt rs863225418(T;T)
Reference Rs863225418(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBXO11 MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033788dupT
CLNSRC
CLNACC RCV000202009.1,