SNP Report

Basic Info

Name	rs5906893 dbSNP Ensembl
Location	chrX:43668376 - 43668376(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.416689
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000338702, ENST00000497485, ENST00000542639); non_coding_transcript_variant(ENST00000497485)
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)
MAOA	monoamine oxidase A	Xp11.4-p11.3	21(10/11/0)

SNPs in LD with rs5906893 (count: 0) View in gBrowse (chrX:43668376..43668376 )

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

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