SNP Report

Basic Info

Name	rs7679284 dbSNP Ensembl
Location	chr4:94531895 - 94531895(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.311701
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000317968, ENST00000318007, ENST00000380180, ENST00000437932, ENST00000503974, ENST00000508216, ENST00000508531, ENST00000509333, ENST00000509357, ENST00000510099, ENST00000511767, ENST00000513341, ENST00000514743, ENST00000514830, ENST00000542407, ENST00000615540, ENST00000627587); NMD_transcript_variant(ENST00000509357, ENST00000627587); non_coding_transcript_variant(ENST00000508531, ENST00000509333, ENST00000511767, ENST00000514830)
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)
PDLIM5	PDZ and LIM domain 5	4q22	5(4/1/0)

SNPs in LD with rs7679284 (count: 0) View in gBrowse (chr4:94531895..94531895 )

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

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