SNP Report

Basic Info

Name	rs10047085 dbSNP Ensembl
Location	chr1:31429571 - 31429571(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.430511
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 rs10047085 (count: 0) View in gBrowse (chr1:31429571..31429571 )

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

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