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)