rs1007637
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1007637(A;A) |
Make rs1007637(A;G) |
Make rs1007637(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 3914315 |
Gene | P2RX1 |
is a | snp |
is | mentioned by |
dbSNP | rs1007637 |
dbSNP (classic) | rs1007637 |
ClinGen | rs1007637 |
ebi | rs1007637 |
HLI | rs1007637 |
Exac | rs1007637 |
Gnomad | rs1007637 |
Varsome | rs1007637 |
LitVar | rs1007637 |
Map | rs1007637 |
PheGenI | rs1007637 |
Biobank | rs1007637 |
1000 genomes | rs1007637 |
hgdp | rs1007637 |
ensembl | rs1007637 |
geneview | rs1007637 |
scholar | rs1007637 |
rs1007637 | |
pharmgkb | rs1007637 |
gwascentral | rs1007637 |
openSNP | rs1007637 |
23andMe | rs1007637 |
SNPshot | rs1007637 |
SNPdbe | rs1007637 |
MSV3d | rs1007637 |
GWAS Ctlg | rs1007637 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 27276213] Functional Characterization of Schizophrenia-Associated Variation in CACNA1C.