SNP Report

Basic Info

Name	rs9616393 dbSNP Ensembl
Location	chr22:49921161 - 49921161(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.11262
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000328268, ENST00000403427, ENST00000404488, ENST00000407217, ENST00000450207, ENST00000482956, ENST00000483652); non_coding_transcript_variant(ENST00000482956, ENST00000483652); upstream_gene_variant(ENST00000330817, ENST00000444954, ENST00000462253, ENST00000487969, ENST00000498354)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ALG12	ALG12, alpha-1,6-mannosyltransferase	22q13.33	Mapped by LD-proxy
CRELD2	cysteine-rich with EGF-like domains 2	22q13.33	Mapped by LD-proxy

SNPs in LD with rs9616393 (count: 0) View in gBrowse (chr22:49921161..49921161 )

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

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