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

rs16856202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16856202(G;G)
Make rs16856202(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position232019405
GeneDISC1, MAP1LC3C
is asnp
is mentioned by
dbSNPrs16856202
ebirs16856202
HLIrs16856202
Exacrs16856202
Varsomers16856202
Maprs16856202
PheGenIrs16856202
hapmaprs16856202
1000 genomesrs16856202
hgdprs16856202
ensemblrs16856202
gopubmedrs16856202
geneviewrs16856202
scholarrs16856202
googlers16856202
pharmgkbrs16856202
gwascentralrs16856202
openSNPrs16856202
23andMers16856202
23andMe allrs16856202
SNP Nexus

SNPshotrs16856202
SNPdbers16856202
MSV3drs16856202
GWAS Ctlgrs16856202
GMAF0.07163
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19451621OA-icon.png]
Trait Amyotrophic lateral sclerosis
Title Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis
Risk Allele A
P-val 0.000008
Odds Ratio 2.00 [NR]


GET Evidence
rs16856202
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.03125
summary