SNP Report

Basic Info

Name	rs17101042 dbSNP Ensembl
Location	chr14:33413870 - 33413870(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.158746
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000346562, ENST00000356141, ENST00000357798, ENST00000546849, ENST00000547068, ENST00000548645, ENST00000549770, ENST00000551008, ENST00000551492, ENST00000551634); non_coding_transcript_variant(ENST00000549770)
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)
NPAS3	neuronal PAS domain protein 3	14q13.1	2(1/1/0)

SNPs in LD with rs17101042 (count: 0) View in gBrowse (chr14:33413870..33413870 )

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

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