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rs17027230

From SNPedia

Orientationplus
Stabilizedplus
Make rs17027230(C;C)
Make rs17027230(C;T)
Make rs17027230(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position102462870
is asnp
is mentioned by
dbSNPrs17027230
ebirs17027230
HLIrs17027230
Exacrs17027230
Varsomers17027230
Maprs17027230
PheGenIrs17027230
hapmaprs17027230
1000 genomesrs17027230
hgdprs17027230
ensemblrs17027230
gopubmedrs17027230
geneviewrs17027230
scholarrs17027230
googlers17027230
pharmgkbrs17027230
gwascentralrs17027230
openSNPrs17027230
23andMers17027230
23andMe allrs17027230
SNP Nexus

SNPshotrs17027230
SNPdbers17027230
MSV3drs17027230
GWAS Ctlgrs17027230
GMAF0.2727
Max Magnitude
? (C;C) (C;T) (T;T) 28

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