SNP Report

Basic Info

Name	rs7290696 dbSNP Ensembl
Location	chr22:31945698 - 31945698(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.148163
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000248975, ENST00000397492, ENST00000443669, ENST00000471374, ENST00000479649); NMD_transcript_variant(ENST00000443669); non_coding_transcript_variant(ENST00000471374, ENST00000479649); upstream_gene_variant(ENST00000420430, ENST00000486651, ENST00000623735)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
C22orf24	chromosome 22 open reading frame 24	22q12.1-q12.3	Mapped by Literature SNP
YWHAH	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta	22q12.1-q13.1	3(2/0/1)

SNPs in LD with rs7290696 (count: 0) View in gBrowse (chr22:31945698..31945698 )

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

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