SNP Report

Basic Info

Name	rs214966 dbSNP Ensembl
Location	chr6:152457463 - 152457463(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.191693
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000498751, ENST00000535896); intron_variant(ENST00000341594, ENST00000367248, ENST00000367253, ENST00000367255, ENST00000413186, ENST00000423061, ENST00000461872, ENST00000474655, ENST00000495090); NMD_transcript_variant(ENST00000474655); non_coding_transcript_variant(ENST00000461872)
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 rs214966 (count: 0) View in gBrowse (chr6:152457463..152457463 )

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

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