SNP Report

Basic Info

Name	rs17485889 dbSNP Ensembl
Location	chr1:168049602 - 168049602(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.177516
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000312263, ENST00000367840, ENST00000367843, ENST00000432587, ENST00000478668, ENST00000489398); non_coding_transcript_variant(ENST00000478668, ENST00000489398)
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)
DCAF6	DDB1 and CUL4 associated factor 6	1q23.3	1(0/1/0)

SNPs in LD with rs17485889 (count: 0) View in gBrowse (chr1:168049602..168049602 )

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

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