SNP Report

Basic Info

Name	rs4627097 dbSNP Ensembl
Location	chr11:125582418 - 125582418(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.340455
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; NMD_transcript_variant; non_coding_transcript_variant; splice_region_variant; synonymous_variant. Polyphen Annotation: benign(ENST00000527235) SIFT Annotation: tolerated - low confidence(ENST00000527235)
Consequence to Transcript	3_prime_UTR_variant(ENST00000531636); downstream_gene_variant(ENST00000524723, ENST00000527131, ENST00000527520, ENST00000527842, ENST00000529765, ENST00000530540); intron_variant(ENST00000530526); missense_variant(ENST00000527235); NMD_transcript_variant(ENST00000531636); non_coding_transcript_variant(ENST00000530526); splice_region_variant(ENST00000527235, ENST00000278903, ENST00000531636, ENST00000534546, ENST00000615917, ENST00000618552, ENST00000620753); synonymous_variant(ENST00000278903, ENST00000534546, ENST00000615917, ENST00000618552, ENST00000620753)
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)
EI24	etoposide induced 2.4	11q24.2	Mapped by LD-proxy
STT3A-AS1	STT3A antisense RNA 1	11q24.2	Mapped by LD-proxy

SNPs in LD with rs4627097 (count: 0) View in gBrowse (chr11:125582418..125582418 )

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

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