SNP Report

Basic Info

Name	rs2022268 dbSNP Ensembl
Location	chr6:83563707 - 83563707(1)
Variant Alleles	G/T
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.183107
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000195649, ENST00000369694, ENST00000439399, ENST00000518312, ENST00000520213, ENST00000520302, ENST00000521485, ENST00000521616, ENST00000521743, ENST00000523448); NMD_transcript_variant(ENST00000518312, ENST00000521616)
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)
SNAP91	synaptosomal-associated protein, 91kDa	6q15	Mapped by LD-proxy

SNPs in LD with rs2022268 (count: 0) View in gBrowse (chr6:83563707..83563707 )

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

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