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rs766325

From SNPedia

Orientationplus
Stabilizedplus
Make rs766325(A;A)
Make rs766325(A;G)
Make rs766325(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position18629964
GenePAX7
is asnp
is mentioned by
dbSNPrs766325
ebirs766325
HLIrs766325
Exacrs766325
Varsomers766325
Maprs766325
PheGenIrs766325
hapmaprs766325
1000 genomesrs766325
hgdprs766325
ensemblrs766325
gopubmedrs766325
geneviewrs766325
scholarrs766325
googlers766325
pharmgkbrs766325
gwascentralrs766325
openSNPrs766325
23andMers766325
23andMe allrs766325
SNP Nexus

SNPshotrs766325
SNPdbers766325
MSV3drs766325
GWAS Ctlgrs766325
GMAF0.4954
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19142206OA-icon.png] Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations


[PMID 23463464OA-icon.png] Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).