SNP Report

Basic Info

Name	rs6004652 dbSNP Ensembl
Location	chr22:25452844 - 25452844(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.116214
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000382734); non_coding_transcript_variant(ENST00000382734); upstream_gene_variant(ENST00000354451, ENST00000415709, ENST00000509460, ENST00000615588)
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)
CRYBB2P1	crystallin, beta B2 pseudogene 1	22q11.2-q12.1	1(0/0/1)

SNPs in LD with rs6004652 (count: 0) View in gBrowse (chr22:25452844..25452844 )

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

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