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rs3798696

From SNPedia

Orientationminus
Stabilizedminus
Make rs3798696(A;A)
Make rs3798696(A;G)
Make rs3798696(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position10403417
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs3798696
ebirs3798696
HLIrs3798696
Exacrs3798696
Varsomers3798696
Maprs3798696
PheGenIrs3798696
hapmaprs3798696
1000 genomesrs3798696
hgdprs3798696
ensemblrs3798696
gopubmedrs3798696
geneviewrs3798696
scholarrs3798696
googlers3798696
pharmgkbrs3798696
gwascentralrs3798696
openSNPrs3798696
23andMers3798696
23andMe allrs3798696
SNP Nexus

SNPshotrs3798696
SNPdbers3798696
MSV3drs3798696
GWAS Ctlgrs3798696
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 3E-6
Odds Ratio NR NR