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rs10192369

From SNPedia

Orientationplus
Stabilizedplus
Make rs10192369(A;A)
Make rs10192369(A;G)
Make rs10192369(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position160524377
is asnp
is mentioned by
dbSNPrs10192369
ebirs10192369
HLIrs10192369
Exacrs10192369
Varsomers10192369
Maprs10192369
PheGenIrs10192369
hapmaprs10192369
1000 genomesrs10192369
hgdprs10192369
ensemblrs10192369
gopubmedrs10192369
geneviewrs10192369
scholarrs10192369
googlers10192369
pharmgkbrs10192369
gwascentralrs10192369
openSNPrs10192369
23andMers10192369
23andMe allrs10192369
SNP Nexus

SNPshotrs10192369
SNPdbers10192369
MSV3drs10192369
GWAS Ctlgrs10192369
GMAF0.4917
Max Magnitude
? (A;A) (A;G) (G;G) 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 T
P-val 0.000009
Odds Ratio 1.17 [NR]


GET Evidence
rs10192369
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.491935
summary