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rs16984239

From SNPedia

Orientationplus
Stabilizedplus
Make rs16984239(A;A)
Make rs16984239(A;C)
Make rs16984239(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position18053180
is asnp
is mentioned by
dbSNPrs16984239
dbSNP (classic)rs16984239
ClinGenrs16984239
ebirs16984239
HLIrs16984239
Exacrs16984239
Gnomadrs16984239
Varsomers16984239
LitVarrs16984239
Maprs16984239
PheGenIrs16984239
Biobankrs16984239
1000 genomesrs16984239
hgdprs16984239
ensemblrs16984239
geneviewrs16984239
scholarrs16984239
googlers16984239
pharmgkbrs16984239
gwascentralrs16984239
openSNPrs16984239
23andMers16984239
SNPshotrs16984239
SNPdbers16984239
MSV3drs16984239
GWAS Ctlgrs16984239
GMAF0.1694
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS
SNP rs16984239
PubMedID [PMID 17362836]
Condition Amyotrophic lateral sclerosis
Gene Intergenic
Risk Allele
pValue 2.00E-006
OR 2.1
95% CI 1.50-3.00


[PMID 19740415OA-icon.png] Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis



[PMID 20823317OA-icon.png] is-rSNP: a novel technique for in silico regulatory SNP detection.