SNP Report

Basic Info

Name	rs2297884 dbSNP Ensembl
Location	chr1:31428805 - 31428805(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.420128
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000487207); intron_variant(ENST00000373709, ENST00000373710, ENST00000491976, ENST00000536384, ENST00000536859); non_coding_transcript_variant(ENST00000491976)
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)
SERINC2	serine incorporator 2	1p35.1	Mapped by LD-proxy

SNPs in LD with rs2297884 (count: 0) View in gBrowse (chr1:31428805..31428805 )

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

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