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

rs797821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797821(A;G)
Make rs797821(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position83961536
GeneSEMA3A
is asnp
is mentioned by
dbSNPrs797821
ebirs797821
HLIrs797821
Exacrs797821
Varsomers797821
Maprs797821
PheGenIrs797821
hapmaprs797821
1000 genomesrs797821
hgdprs797821
ensemblrs797821
gopubmedrs797821
geneviewrs797821
scholarrs797821
googlers797821
pharmgkbrs797821
gwascentralrs797821
openSNPrs797821
23andMers797821
23andMe allrs797821
SNP Nexus

SNPshotrs797821
SNPdbers797821
MSV3drs797821
GWAS Ctlgrs797821
GMAF0.3779
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


ClinVar
Risk rs797821(G;G)
Alt rs797821(G;G)
Reference rs797821(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene SEMA3A
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.83590852T>C
CLNSRC
CLNACC RCV000175195.1,