SNP Report

Basic Info

Name	rs7763880 dbSNP Ensembl
Location	chr6:152481162 - 152481162(1)
Variant Alleles	T/C
Ancestral Allele	A
Minor Allele	T
Minor Allele Frequence	0.395966
Functional Annotation	intron_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: benign(ENST00000341594)
Consequence to Transcript	intron_variant(ENST00000367248, ENST00000367253, ENST00000367255, ENST00000413186, ENST00000423061, ENST00000461872, ENST00000466159, ENST00000537750, ENST00000610489); missense_variant(ENST00000341594); non_coding_transcript_exon_variant(ENST00000535896); 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 rs7763880 (count: 0) View in gBrowse (chr6:152481162..152481162 )

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

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