SNP Report

Basic Info

Name	rs4949449 dbSNP Ensembl
Location	chr1:31622933 - 31622933(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.440895
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000373705, ENST00000373706, ENST00000403528, ENST00000468521, ENST00000485464); non_coding_transcript_variant(ENST00000468521, ENST00000485464)
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)
HCRTR1	hypocretin (orexin) receptor 1	1p33	1(1/0/0)

SNPs in LD with rs4949449 (count: 0) View in gBrowse (chr1:31622933..31622933 )

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

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