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rs988213

From SNPedia

Orientationplus
Stabilizedplus
Make rs988213(A;A)
Make rs988213(A;G)
Make rs988213(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position46545004
GeneLOXHD1
is asnp
is mentioned by
dbSNPrs988213
dbSNP (classic)rs988213
ClinGenrs988213
ebirs988213
HLIrs988213
Exacrs988213
Gnomadrs988213
Varsomers988213
LitVarrs988213
Maprs988213
PheGenIrs988213
Biobankrs988213
1000 genomesrs988213
hgdprs988213
ensemblrs988213
geneviewrs988213
scholarrs988213
googlers988213
pharmgkbrs988213
gwascentralrs988213
openSNPrs988213
23andMers988213
23andMe allrs988213
SNPshotrs988213
SNPdbers988213
MSV3drs988213
GWAS Ctlgrs988213
GMAF0.3714
Max Magnitude0
? (A;A) (A;G) (G;G) 28


This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]