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rs16976358

From SNPedia

Orientationplus
Make rs16976358(C;C)
Make rs16976358(C;T)
Make rs16976358(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position42611606
GeneLINC00907
is asnp
is mentioned by
dbSNPrs16976358
ebirs16976358
HLIrs16976358
Exacrs16976358
Varsomers16976358
Maprs16976358
PheGenIrs16976358
hapmaprs16976358
1000 genomesrs16976358
hgdprs16976358
ensemblrs16976358
gopubmedrs16976358
geneviewrs16976358
scholarrs16976358
googlers16976358
pharmgkbrs16976358
gwascentralrs16976358
openSNPrs16976358
23andMers16976358
23andMe allrs16976358
SNP Nexus

SNPshotrs16976358
SNPdbers16976358
MSV3drs16976358
GWAS Ctlgrs16976358
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26314684] Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations