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)