SNP Report

Basic Info

Name	rs1565756 dbSNP Ensembl
Location	chr15:77449298 - 77449298(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.461062
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000336216, ENST00000381714, ENST00000558176, ENST00000558651, ENST00000559035, ENST00000559099, ENST00000560498, ENST00000560986); NMD_transcript_variant(ENST00000559035); non_coding_transcript_variant(ENST00000560986)
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)
HMG20A	high mobility group 20A	15q24	1(1/0/0)

SNPs in LD with rs1565756 (count: 0) View in gBrowse (chr15:77449298..77449298 )

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

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