SNP Report

Basic Info

Name	rs5996945 dbSNP Ensembl
Location	chr22:25479606 - 25479606(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.260383
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000354451, ENST00000509460); non_coding_transcript_exon_variant(ENST00000609475); non_coding_transcript_variant(ENST00000354451, ENST00000509460, ENST00000609475)
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 rs5996945 (count: 0) View in gBrowse (chr22:25479606..25479606 )

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

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