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)