SNP Report

Basic Info
Name rs214961 dbSNP Ensembl
Location chr6:152460604 - 152460604(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele A
Minor Allele Frequence 0.393371
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000466159, ENST00000468937, ENST00000481502, ENST00000498751, ENST00000537750); intron_variant(ENST00000341594, ENST00000367248, ENST00000367253, ENST00000367255, ENST00000413186, ENST00000423061, ENST00000461872, ENST00000474655, ENST00000495090, ENST00000535896); NMD_transcript_variant(ENST00000474655); non_coding_transcript_variant(ENST00000461872, ENST00000535896)
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)
SYNE1 spectrin repeat containing, nuclear envelope 1 6q25.2 6(3/2/1)

SNPs in LD with rs214961 (count: 0) View in gBrowse (chr6:152460604..152460604 )

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

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