SNP Report

Basic Info
Name rs3818888 dbSNP Ensembl
Location chr1:147659595 - 147659595(1)
Variant Alleles A/C
Ancestral Allele A
Minor Allele C
Minor Allele Frequence 0.132987
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000392988, ENST00000487562, ENST00000493129, ENST00000583509, ENST00000611629, ENST00000613673, ENST00000620634); NMD_transcript_variant(ENST00000620634); non_coding_transcript_variant(ENST00000613673); upstream_gene_variant(ENST00000609196, ENST00000614551)
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)
ACP6 acid phosphatase 6, lysophosphatidic 1q21 1(1/0/0)

SNPs in LD with rs3818888 (count: 0) View in gBrowse (chr1:147659595..147659595 )

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

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