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rs9971637

From SNPedia

Orientationplus
Stabilizedplus
Make rs9971637(A;A)
Make rs9971637(A;G)
Make rs9971637(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position17220805
is asnp
is mentioned by
dbSNPrs9971637
ebirs9971637
HLIrs9971637
Exacrs9971637
Varsomers9971637
Maprs9971637
PheGenIrs9971637
hapmaprs9971637
1000 genomesrs9971637
hgdprs9971637
ensemblrs9971637
gopubmedrs9971637
geneviewrs9971637
scholarrs9971637
googlers9971637
pharmgkbrs9971637
gwascentralrs9971637
openSNPrs9971637
23andMers9971637
23andMe allrs9971637
SNP Nexus

SNPshotrs9971637
SNPdbers9971637
MSV3drs9971637
GWAS Ctlgrs9971637
GMAF0.1253
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 0.000002
Odds Ratio 1.48 [NR]


GET Evidence
rs9971637
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.198413
summary