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rs7577894

From SNPedia

Orientationplus
Stabilizedplus
Make rs7577894(C;C)
Make rs7577894(C;T)
Make rs7577894(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position55781769
is asnp
is mentioned by
dbSNPrs7577894
ebirs7577894
HLIrs7577894
Exacrs7577894
Varsomers7577894
Maprs7577894
PheGenIrs7577894
hapmaprs7577894
1000 genomesrs7577894
hgdprs7577894
ensemblrs7577894
gopubmedrs7577894
geneviewrs7577894
scholarrs7577894
googlers7577894
pharmgkbrs7577894
gwascentralrs7577894
openSNPrs7577894
23andMers7577894
23andMe allrs7577894
SNP Nexus

SNPshotrs7577894
SNPdbers7577894
MSV3drs7577894
GWAS Ctlgrs7577894
GMAF0.3898
Max Magnitude
? (C;C) (C;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 T
P-val 0.000001
Odds Ratio 1.41 [NR]


GET Evidence
rs7577894
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.619048
summary