SNP Report

Basic Info

Name	rs483978 dbSNP Ensembl
Location	chr4:55394922 - 55394922(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.265575
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000592823, ENST00000598819, ENST00000599135, ENST00000601433, ENST00000608136); non_coding_transcript_variant(ENST00000592823, ENST00000598819, ENST00000599135, ENST00000601433, ENST00000608136); upstream_gene_variant(ENST00000381334, ENST00000506198, ENST00000508404, ENST00000511710, ENST00000514070)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
TMEM165	transmembrane protein 165	4q12	Mapped by Literature SNP
SRD5A3-AS1	SRD5A3 antisense RNA 1	4q12	Mapped by LD-proxy

SNPs in LD with rs483978 (count: 0) View in gBrowse (chr4:55394922..55394922 )

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

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