SNP Report

Basic Info

Name	rs2464978 dbSNP Ensembl
Location	chr2:207593194 - 207593194(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0950479
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000353267, ENST00000418081, ENST00000425132, ENST00000430624, ENST00000432329, ENST00000432416, ENST00000448277, ENST00000458426, ENST00000494983); NMD_transcript_variant(ENST00000418081); non_coding_transcript_variant(ENST00000494983); upstream_gene_variant(ENST00000446449, ENST00000451164)
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)
CREB1	cAMP responsive element binding protein 1	2q34	2(1/1/0)
METTL21A	methyltransferase like 21A	2q33.3	Mapped by Literature SNP

SNPs in LD with rs2464978 (count: 0) View in gBrowse (chr2:207593194..207593194 )

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

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