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rs5937496

From SNPedia

Orientationplus
Stabilizedplus
Make rs5937496(A;A)
Make rs5937496(A;G)
Make rs5937496(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position76127599
is asnp
is mentioned by
dbSNPrs5937496
ebirs5937496
HLIrs5937496
Exacrs5937496
Varsomers5937496
Maprs5937496
PheGenIrs5937496
hapmaprs5937496
1000 genomesrs5937496
hgdprs5937496
ensemblrs5937496
gopubmedrs5937496
geneviewrs5937496
scholarrs5937496
googlers5937496
pharmgkbrs5937496
gwascentralrs5937496
openSNPrs5937496
23andMers5937496
23andMe allrs5937496
SNP Nexus

SNPshotrs5937496
SNPdbers5937496
MSV3drs5937496
GWAS Ctlgrs5937496
GMAF0.1179
Max Magnitude
? (A;A) (A;G) (G;G) 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 6E-7
Odds Ratio 1.38 [NR]


GET Evidence
rs5937496
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.076087
summary