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rs1366813

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1366813(C;C)
Make rs1366813(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position31347510
GeneXDH
is asnp
is mentioned by
dbSNPrs1366813
ebirs1366813
HLIrs1366813
Exacrs1366813
Varsomers1366813
Maprs1366813
PheGenIrs1366813
hapmaprs1366813
1000 genomesrs1366813
hgdprs1366813
ensemblrs1366813
gopubmedrs1366813
geneviewrs1366813
scholarrs1366813
googlers1366813
pharmgkbrs1366813
gwascentralrs1366813
openSNPrs1366813
23andMers1366813
23andMe allrs1366813
SNP Nexus

SNPshotrs1366813
SNPdbers1366813
MSV3drs1366813
GWAS Ctlgrs1366813
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs1366813(C;C)
Alt rs1366813(C;C)
Reference rs1366813(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene XDH
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.31570376T>C
CLNSRC
CLNACC RCV000171492.1,