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rs17551608

From SNPedia

Orientationplus
Make rs17551608(C;C)
Make rs17551608(C;T)
Make rs17551608(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position168408534
GeneWWC1
is asnp
is mentioned by
dbSNPrs17551608
ebirs17551608
HLIrs17551608
Exacrs17551608
Varsomers17551608
Maprs17551608
PheGenIrs17551608
hapmaprs17551608
1000 genomesrs17551608
hgdprs17551608
ensemblrs17551608
gopubmedrs17551608
geneviewrs17551608
scholarrs17551608
googlers17551608
pharmgkbrs17551608
gwascentralrs17551608
openSNPrs17551608
23andMers17551608
23andMe allrs17551608
SNP Nexus

SNPshotrs17551608
SNPdbers17551608
MSV3drs17551608
GWAS Ctlgrs17551608
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26405221] Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk