SNP Report

Basic Info

Name	rs17605251 dbSNP Ensembl
Location	chrCHR_HSCHR7_1_CTG4_4:103225787 - 103225787(-1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.0686901
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000341533, ENST00000414118, ENST00000417955, ENST00000420631, ENST00000422589, ENST00000427257, ENST00000465647); NMD_transcript_variant(ENST00000420631, ENST00000422589); non_coding_transcript_variant(ENST00000414118, ENST00000631820, ENST00000631940, ENST00000632400, ENST00000632491, ENST00000633207, ENST00000631820, ENST00000631940, ENST00000632400, ENST00000632491, ENST00000633207)
No. of Studies	1 (Positive: 0; Negative: 1; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Pisanu, C., 2013	G/A		logistic regression, P-value=0.337, OR=0.87 logistic regression, P-value=0.337, OR=0.87	Nominal association with BD or lithium response was not obse...... Nominal association with BD or lithium response was not observed in this study. More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NAPEPLD	N-acyl phosphatidylethanolamine phospholipase D	7q22.1	1(1/0/0)

SNPs in LD with rs17605251 (count: 0) View in gBrowse (chrCHR_HSCHR7_1_CTG4_4:103225787..103225787 )

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

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