SNP Report

Basic Info

Name	rs10149544 dbSNP Ensembl
Location	chr14:49694971 - 49694971(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0513179
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000359332, ENST00000553274, ENST00000555704, ENST00000556392, ENST00000557128); NMD_transcript_variant(ENST00000555704, ENST00000556392)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
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
Feng, T.,2010			Fisher's exact tests: Empirical P-value(1, 000, 000 permutat...... Fisher's exact tests: Empirical P-value(1, 000, 000 permutations)=0.000148 More...	Suggestive association was found. Suggestive association was found.	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
KLHDC1	kelch domain containing 1	14q21.3	2(1/0/1)

SNPs in LD with rs10149544 (count: 0) View in gBrowse (chr14:49694971..49694971 )

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

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