SNP Report

Basic Info

Name	rs169631 dbSNP Ensembl
Location	chr12:121145948 - 121145948(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.476438
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000261826, ENST00000328963, ENST00000535250, ENST00000535600, ENST00000535928, ENST00000537312, ENST00000538011, ENST00000539606, ENST00000539695, ENST00000541022, ENST00000541564, ENST00000541716, ENST00000545434); NMD_transcript_variant(ENST00000261826, ENST00000535250, ENST00000535600, ENST00000535928, ENST00000537312, ENST00000538011, ENST00000539606, ENST00000541022, ENST00000541564, ENST00000541716, ENST00000545434); non_coding_transcript_variant(ENST00000539695); upstream_gene_variant(ENST00000407764)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
P2RX7	purinergic receptor P2X, ligand gated ion channel, 7	12q24	9(2/7/0)

SNPs in LD with rs169631 (count: 0) View in gBrowse (chr12:121145948..121145948 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)