SNP Report

Basic Info

Name	rs1367959 dbSNP Ensembl
Location	chr15:26672011 - 26672011(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.246006
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000299267, ENST00000311550, ENST00000541819, ENST00000545868, ENST00000554556, ENST00000555094, ENST00000555632, ENST00000622697, ENST00000628124, ENST00000636466, ENST00000638099); NMD_transcript_variant(ENST00000554556, ENST00000555632); non_coding_transcript_variant(ENST00000555094)
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)
GABRB3	gamma-aminobutyric acid (GABA) A receptor, beta 3	15q12	3(1/2/0)

SNPs in LD with rs1367959 (count: 0) View in gBrowse (chr15:26672011..26672011 )

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

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