SNP Report

Basic Info

Name	rs8041381 dbSNP Ensembl
Location	chr15:60570763 - 60570763(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.354433
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000261523, ENST00000309157, ENST00000335670, ENST00000449337, ENST00000551975, ENST00000557822, ENST00000558234, ENST00000558235, ENST00000559343, ENST00000559824, ENST00000560004); NMD_transcript_variant(ENST00000551975); non_coding_transcript_variant(ENST00000557822, ENST00000558234, ENST00000558235, ENST00000559824, ENST00000560004)
No. of Studies	1 (Positive: 1; Negative: 0; 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
Lai, Y. C., 2015			Empirical P-value=0.022, OR=1.31 Empirical P-value=0.022, OR=1.31	One of 45 SNPs showed associations with BD. One of 45 SNPs showed associations with BD.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RORA	RAR-related orphan receptor A	15q21-q22	3(2/1/0)

SNPs in LD with rs8041381 (count: 0) View in gBrowse (chr15:60570763..60570763 )

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

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