SNP Report

Basic Info

Name	rs11545763 dbSNP Ensembl
Location	chr22:49925522 - 49925522(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.067492
Functional Annotation	downstream_gene_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: possibly damaging(ENST00000403427, ENST00000407217); probably damaging(ENST00000328268, ENST00000404488) SIFT Annotation: deleterious(ENST00000403427, ENST00000407217, ENST00000328268, ENST00000404488)
Consequence to Transcript	downstream_gene_variant(ENST00000444954, ENST00000450207, ENST00000462253, ENST00000482956, ENST00000498354); missense_variant(ENST00000403427, ENST00000407217, ENST00000328268, ENST00000404488); non_coding_transcript_exon_variant(ENST00000483652, ENST00000487969); non_coding_transcript_variant(ENST00000483652, ENST00000487969)
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)
CRELD2	cysteine-rich with EGF-like domains 2	22q13.33	Mapped by LD-proxy

SNPs in LD with rs11545763 (count: 0) View in gBrowse (chr22:49925522..49925522 )

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

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