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rs4810685

From SNPedia

Orientationplus
Stabilizedplus
Make rs4810685(C;C)
Make rs4810685(C;T)
Make rs4810685(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position47771969
GeneSULF2
is asnp
is mentioned by
dbSNPrs4810685
ebirs4810685
HLIrs4810685
Exacrs4810685
Varsomers4810685
Maprs4810685
PheGenIrs4810685
hapmaprs4810685
1000 genomesrs4810685
hgdprs4810685
ensemblrs4810685
gopubmedrs4810685
geneviewrs4810685
scholarrs4810685
googlers4810685
pharmgkbrs4810685
gwascentralrs4810685
openSNPrs4810685
23andMers4810685
23andMe allrs4810685
SNP Nexus

SNPshotrs4810685
SNPdbers4810685
MSV3drs4810685
GWAS Ctlgrs4810685
GMAF0.3678
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18937294OA-icon.png]
Trait Attention deficit hyperactivity disorder (time to onset)
Title Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder
Risk Allele C
P-val 0.000007
Odds Ratio NR NR


[PMID 20148275OA-icon.png] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.


GET Evidence
rs4810685
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.611111
summary