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rs7702057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7702057(G;T)
Make rs7702057(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position116392141
GeneLOC101927212
is asnp
is mentioned by
dbSNPrs7702057
ebirs7702057
HLIrs7702057
Exacrs7702057
Varsomers7702057
Maprs7702057
PheGenIrs7702057
hapmaprs7702057
1000 genomesrs7702057
hgdprs7702057
ensemblrs7702057
gopubmedrs7702057
geneviewrs7702057
scholarrs7702057
googlers7702057
pharmgkbrs7702057
gwascentralrs7702057
openSNPrs7702057
23andMers7702057
23andMe allrs7702057
SNP Nexus

SNPshotrs7702057
SNPdbers7702057
MSV3drs7702057
GWAS Ctlgrs7702057
GMAF0.1511
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 C
P-val 0.000008
Odds Ratio 2.05 [NR]


GET Evidence
rs7702057
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.116279
summary