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

rs2303298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2303298(A;A)
Make rs2303298(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position50623548
GeneNRXN1
is asnp
is mentioned by
dbSNPrs2303298
ebirs2303298
HLIrs2303298
Exacrs2303298
Varsomers2303298
Maprs2303298
PheGenIrs2303298
hapmaprs2303298
1000 genomesrs2303298
hgdprs2303298
ensemblrs2303298
gopubmedrs2303298
geneviewrs2303298
scholarrs2303298
googlers2303298
pharmgkbrs2303298
gwascentralrs2303298
openSNPrs2303298
23andMers2303298
23andMe allrs2303298
SNP Nexus

SNPshotrs2303298
SNPdbers2303298
MSV3drs2303298
GWAS Ctlgrs2303298
GMAF0.05601
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 22405623] Mutation analysis of the NRXN1 gene in a Chinese autism cohort


[PMID 19805132OA-icon.png] Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados.


ClinVar
Risk rs2303298(A;A)
Alt rs2303298(A;A)
Reference rs2303298(G;G)
Significance Other
Disease not specified
Variation info
Gene NRXN1 LOC101927089
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.50850686G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000117844.6,