SNP Report

Basic Info

Name	rs138871 dbSNP Ensembl
Location	chr22:49816226 - 49816226(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.304113
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000459821, ENST00000494833); intron_variant(ENST00000216267, ENST00000404034, ENST00000404760, ENST00000438393, ENST00000457780); NMD_transcript_variant(ENST00000438393); upstream_gene_variant(ENST00000444011)
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)
BRD1	bromodomain containing 1	22q13.33	2(2/0/0)

SNPs in LD with rs138871 (count: 0) View in gBrowse (chr22:49816226..49816226 )

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

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