SNP Report

Basic Info
Name rs7879511 dbSNP Ensembl
Location chrX:53989707 - 53989707(1)
Variant Alleles A/C
Ancestral Allele C
Minor Allele C
Minor Allele Frequence 0.153377
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000413386, ENST00000448003); intron_variant(ENST00000322659, ENST00000338154, ENST00000338946, ENST00000357988, ENST00000396282, ENST00000443302, ENST00000494928); non_coding_transcript_variant(ENST00000494928)
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)
PHF8 PHD finger protein 8 Xp11.22 1(0/0/1)

SNPs in LD with rs7879511 (count: 0) View in gBrowse (chrX:53989707..53989707 )

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

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