SNP Report

Basic Info

Name	rs2069235 dbSNP Ensembl
Location	chr22:39351775 - 39351775(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.496605
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000216155, ENST00000318801, ENST00000328933, ENST00000406293, ENST00000415332, ENST00000489206); NMD_transcript_variant(ENST00000415332); non_coding_transcript_variant(ENST00000489206)
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)
SYNGR1	synaptogyrin 1	22q13	3(2/1/0)

SNPs in LD with rs2069235 (count: 0) View in gBrowse (chr22:39351775..39351775 )

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

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