Rs10503887

From SNPedia
Jump to: navigation, search

Orientationplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10503887(G;T)
Make rs10503887(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position31775931
GeneNRG1
is asnp
is mentioned by
dbSNPrs10503887
Exacrs10503887
PheGenIrs10503887
nextbiors10503887
hapmaprs10503887
1000 genomesrs10503887
hgdprs10503887
ensemblrs10503887
gopubmedrs10503887
geneviewrs10503887
scholarrs10503887
googlers10503887
pharmgkbrs10503887
gwascentralrs10503887
openSNPrs10503887
23andMers10503887
23andMe allrs10503887
SNP Nexus

SNPshotrs10503887
SNPdbers10503887
MSV3drs10503887
GMAF0.1065
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs10503887
PubMedID [PMID 17903296OA-icon.png]
Condition Hip geometry
Gene NRG1
Risk Allele
pValue 2.00E-007
OR NA
95% CI



GET Evidence
rs10503887
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary