SNP Report

Basic Info

Name	rs7214541 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG2:1272807 - 1272807(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.379992
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000264335, ENST00000469398, ENST00000486241, ENST00000489287, ENST00000571732, ENST00000573026, ENST00000573196, ENST00000575977); NMD_transcript_variant(ENST00000573196); non_coding_transcript_variant(ENST00000469398, ENST00000486241, ENST00000489287); upstream_gene_variant(ENST00000466227, ENST00000616643, ENST00000626999, ENST00000627099, ENST00000627231, ENST00000628106, ENST00000630045, ENST00000630606, ENST00000630699, ENST00000630606, ENST00000627099, ENST00000630045, ENST00000630699, ENST00000629090)
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)
YWHAE	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon	17p13.3	1(0/1/0)

SNPs in LD with rs7214541 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG2:1272807..1272807 )

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

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