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rs36026860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs36026860(A;G)
Make rs36026860(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position84005501
GeneSEMA3A
is asnp
is mentioned by
dbSNPrs36026860
ebirs36026860
HLIrs36026860
Exacrs36026860
Varsomers36026860
Maprs36026860
PheGenIrs36026860
hapmaprs36026860
1000 genomesrs36026860
hgdprs36026860
ensemblrs36026860
gopubmedrs36026860
geneviewrs36026860
scholarrs36026860
googlers36026860
pharmgkbrs36026860
gwascentralrs36026860
openSNPrs36026860
23andMers36026860
23andMe allrs36026860
SNP Nexus

SNPshotrs36026860
SNPdbers36026860
MSV3drs36026860
GWAS Ctlgrs36026860
GMAF0.0009183
Max Magnitude0

[PMID 19957197] Candidate gene analysis of semaphorins in patients with Alzheimer's disease

ClinVar
Risk rs36026860(G;G)
Alt rs36026860(G;G)
Reference rs36026860(A;A)
Significance Untested
Disease not provided
Variation info
Gene SEMA3A
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.83634817T>C
CLNSRC UniProtKB (variants)
CLNACC RCV000059787.1,


[PMID 22927827OA-icon.png] SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.