Have questions? Visit https://www.reddit.com/r/SNPedia

rs7632000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs7632000(C;T)
Make rs7632000(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position4662253
GeneITPR1
is asnp
is mentioned by
dbSNPrs7632000
dbSNP (old)rs7632000
ClinGenrs7632000
ebirs7632000
HLIrs7632000
Exacrs7632000
Gnomadrs7632000
Varsomers7632000
Maprs7632000
PheGenIrs7632000
Biobankrs7632000
1000 genomesrs7632000
hgdprs7632000
ensemblrs7632000
gopubmedrs7632000
geneviewrs7632000
scholarrs7632000
googlers7632000
pharmgkbrs7632000
gwascentralrs7632000
openSNPrs7632000
23andMers7632000
23andMe allrs7632000
SNP Nexus

SNPshotrs7632000
SNPdbers7632000
MSV3drs7632000
GWAS Ctlgrs7632000
Max Magnitude0
GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele A
P-val 7E-7
Odds Ratio .03 [NR] pg/mL increase


ClinVar
Risk rs7632000(G;G) rs7632000(T;T)
Alt rs7632000(G;G) rs7632000(T;T)
Reference Rs7632000(C;C)
Significance Probable-non-pathogenic
Disease Spinocerebellar Ataxia
Variation info
Gene ITPR1
CLNDBN Spinocerebellar Ataxia, Dominant
Reversed 0
HGVS NC_000003.11:g.4703937C>T
CLNSRC
CLNACC RCV000286031.1,