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

rs774359

From SNPedia

Orientationplus
Stabilizedplus
Make rs774359(C;C)
Make rs774359(C;T)
Make rs774359(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position27561051
GeneC9orf72
is asnp
is mentioned by
dbSNPrs774359
ebirs774359
HLIrs774359
Exacrs774359
Varsomers774359
Maprs774359
PheGenIrs774359
hapmaprs774359
1000 genomesrs774359
hgdprs774359
ensemblrs774359
gopubmedrs774359
geneviewrs774359
scholarrs774359
googlers774359
pharmgkbrs774359
gwascentralrs774359
openSNPrs774359
23andMers774359
23andMe allrs774359
SNP Nexus

SNPshotrs774359
SNPdbers774359
MSV3drs774359
GWAS Ctlgrs774359
GMAF0.1997
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19734901]
Trait Amyotrophic lateral sclerosis
Title Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Risk Allele
P-val 0.000003
Odds Ratio 1.19 [NR]



[PMID 20423481OA-icon.png] Lack of replication of genetic predictors for the rheumatoid arthritis response to anti-TNF treatments: a prospective case-only study.


GET Evidence
rs774359
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary