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rs863225420

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225420(C;G)
Make rs863225420(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806805
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs863225420
ebirs863225420
HLIrs863225420
Exacrs863225420
Varsomers863225420
Maprs863225420
PheGenIrs863225420
hapmaprs863225420
1000 genomesrs863225420
hgdprs863225420
ensemblrs863225420
gopubmedrs863225420
geneviewrs863225420
scholarrs863225420
googlers863225420
pharmgkbrs863225420
gwascentralrs863225420
openSNPrs863225420
23andMers863225420
23andMe allrs863225420
SNP Nexus

SNPshotrs863225420
SNPdbers863225420
MSV3drs863225420
GWAS Ctlgrs863225420
Max Magnitude0
ClinVar
Risk rs863225420(G;G)
Alt rs863225420(G;G)
Reference rs863225420(C;C)
Significance Pathogenic
Disease not provided Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN not provided Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033944C>G
CLNSRC
CLNACC RCV000202283.1, RCV000204963.1,