SNP Report

Basic Info

Name	rs7698022 dbSNP Ensembl
Location	chr4:55541180 - 55541180(1)
Variant Alleles	G/T
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.229433
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000381322, ENST00000435527, ENST00000506923, ENST00000509151, ENST00000513033, ENST00000513440); non_coding_transcript_variant(ENST00000506923, ENST00000509151, ENST00000513033); upstream_gene_variant(ENST00000411373)
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)
RN7SKP30	RNA, 7SK small nuclear pseudogene 30	4q12	Mapped by Literature SNP
CLOCK	clock circadian regulator	4q12	12(5/7/0)

SNPs in LD with rs7698022 (count: 0) View in gBrowse (chr4:55541180..55541180 )

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

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