SNP Report

Basic Info

Name	rs61730283 dbSNP Ensembl
Location	chr12:38321127 - 38321127(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.014976
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; NMD_transcript_variant. Polyphen Annotation: benign(ENST00000308742) SIFT Annotation: tolerated(ENST00000308742)
Consequence to Transcript	3_prime_UTR_variant(ENST00000548240); downstream_gene_variant(ENST00000553138); intron_variant(ENST00000551464); missense_variant(ENST00000308742); NMD_transcript_variant(ENST00000548240)
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
Strauss, K. A., 2014	A/G		Bipolar 1 disorder: X²=1.4, FBAT P-value=0.276, E...... Bipolar 1 disorder: X²=1.4, FBAT P-value=0.276, EMMAX P-value=0.194; Bipolar spectrum disorder: X⁶=0.9, FBAT P-value=0.599, EMMAX P-value=0.651 More...	No significant associations were observed. No significant associations were observed.	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ALG10B	ALG10B, alpha-1,2-glucosyltransferase	12q12	1(0/1/0)

SNPs in LD with rs61730283 (count: 0) View in gBrowse (chr12:38321127..38321127 )

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

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