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rs7801303

From SNPedia

Orientationplus
Stabilizedplus
Make rs7801303(A;A)
Make rs7801303(A;G)
Make rs7801303(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position40878471
is asnp
is mentioned by
dbSNPrs7801303
ebirs7801303
HLIrs7801303
Exacrs7801303
Varsomers7801303
Maprs7801303
PheGenIrs7801303
hapmaprs7801303
1000 genomesrs7801303
hgdprs7801303
ensemblrs7801303
gopubmedrs7801303
geneviewrs7801303
scholarrs7801303
googlers7801303
pharmgkbrs7801303
gwascentralrs7801303
openSNPrs7801303
23andMers7801303
23andMe allrs7801303
SNP Nexus

SNPshotrs7801303
SNPdbers7801303
MSV3drs7801303
GWAS Ctlgrs7801303
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24571439OA-icon.png]
Trait Parent of origin effect on language impairment (paternal)
Title Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Risk Allele
P-val 4E-7
Odds Ratio NR NR