SNP Report

Basic Info

Name	rs214976 dbSNP Ensembl
Location	chr6:152451129 - 152451129(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.392772
Functional Annotation	downstream_gene_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: benign(ENST00000367248, ENST00000367253, ENST00000413186, ENST00000367255, ENST00000423061); possibly damaging(ENST00000341594) SIFT Annotation: deleterious(ENST00000367248, ENST00000367253, ENST00000413186)
Consequence to Transcript	downstream_gene_variant(ENST00000474655, ENST00000495090); missense_variant(ENST00000367248, ENST00000367253, ENST00000413186, ENST00000367255, ENST00000423061, ENST00000341594); non_coding_transcript_exon_variant(ENST00000461872); 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 rs214976 (count: 0) View in gBrowse (chr6:152451129..152451129 )

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

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