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rs3752433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3752433(C;T)
Make rs3752433(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position22221603
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs3752433
dbSNP (old)rs3752433
ClinGenrs3752433
ebirs3752433
HLIrs3752433
Exacrs3752433
Varsomers3752433
Maprs3752433
PheGenIrs3752433
Biobankrs3752433
1000 genomesrs3752433
hgdprs3752433
ensemblrs3752433
gopubmedrs3752433
geneviewrs3752433
scholarrs3752433
googlers3752433
pharmgkbrs3752433
gwascentralrs3752433
openSNPrs3752433
23andMers3752433
23andMe allrs3752433
SNP Nexus

SNPshotrs3752433
SNPdbers3752433
MSV3drs3752433
GWAS Ctlgrs3752433
Max Magnitude0
GWAS snp
PMID [PMID 24489884OA-icon.png]
Trait Anger
Title Genome-wide association study of proneness to anger.
Risk Allele A
P-val 3E-7
Odds Ratio .15 [NR] unit increase


ClinVar
Risk rs3752433(T;T)
Alt rs3752433(T;T)
Reference Rs3752433(C;C)
Significance Non-pathogenic
Disease not specified Familial X-linked hypophosphatemic vitamin D refractory rickets
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not specified Familial X-linked hypophosphatemic vitamin D refractory rickets
Reversed 0
HGVS NC_000023.10:g.22239720C>T
CLNSRC
CLNACC RCV000244555.1, RCV000286035.1,