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rs7804122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7804122(A;G)
Make rs7804122(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position84005397
GeneSEMA3A
is asnp
is mentioned by
dbSNPrs7804122
ebirs7804122
HLIrs7804122
Exacrs7804122
Varsomers7804122
Maprs7804122
PheGenIrs7804122
hapmaprs7804122
1000 genomesrs7804122
hgdprs7804122
ensemblrs7804122
gopubmedrs7804122
geneviewrs7804122
scholarrs7804122
googlers7804122
pharmgkbrs7804122
gwascentralrs7804122
openSNPrs7804122
23andMers7804122
23andMe allrs7804122
SNP Nexus

SNPshotrs7804122
SNPdbers7804122
MSV3drs7804122
GWAS Ctlgrs7804122
GMAF0.2107
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 22184102] SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of China