SNP Report

Basic Info

Name	rs6271 dbSNP Ensembl
Location	chr9:133657152 - 133657152(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0207668
Functional Annotation	missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: possibly damaging(ENST00000393056) SIFT Annotation: tolerated(ENST00000393056)
Consequence to Transcript	missense_variant(ENST00000393056); non_coding_transcript_exon_variant(ENST00000425189); non_coding_transcript_variant(ENST00000425189)
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
Ates, O.,2013	G/A		Genotypic P-value = 0.8850;allelic P-value = 0.348 Genotypic P-value = 0.8850;allelic P-value = 0.348	There was no association observed between the genotype and a...... There was no association observed between the genotype and allelic frequencies for 444G>A polymorphism and bipolar disorder. More...	Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DBH	dopamine beta-hydroxylase (dopamine beta-monooxygenase)	9q34	3(1/2/0)
DBH-AS1	DBH antisense RNA 1	9q34.2	Mapped by Literature SNP

SNPs in LD with rs6271 (count: 0) View in gBrowse (chr9:133657152..133657152 )

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

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