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rs863223913

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223913(A;A)
Make rs863223913(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position91217305
GeneAUH
is asnp
is mentioned by
dbSNPrs863223913
ebirs863223913
HLIrs863223913
Exacrs863223913
Varsomers863223913
Maprs863223913
PheGenIrs863223913
hapmaprs863223913
1000 genomesrs863223913
hgdprs863223913
ensemblrs863223913
gopubmedrs863223913
geneviewrs863223913
scholarrs863223913
googlers863223913
pharmgkbrs863223913
gwascentralrs863223913
openSNPrs863223913
23andMers863223913
23andMe allrs863223913
SNP Nexus

SNPshotrs863223913
SNPdbers863223913
MSV3drs863223913
GWAS Ctlgrs863223913
Max Magnitude0
ClinVar
Risk rs863223913(A;A)
Alt rs863223913(A;A)
Reference rs863223913(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AUH
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.93979587G>T
CLNSRC
CLNACC RCV000197701.1,