SNP Report

Basic Info

Name	rs11562929 dbSNP Ensembl
Location	chr4:117688080 - 117688080(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.16234
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000422145, ENST00000600624, ENST00000626258, ENST00000630321); non_coding_transcript_variant(ENST00000422145, ENST00000600624, ENST00000626258, ENST00000630321)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs11562929 (count: 0) View in gBrowse (chr4:117688080..117688080 )

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

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