SNP Report

Basic Info

Name	rs35003670 dbSNP Ensembl
Location	chr9:114424482 - 114424482(1)
Variant Alleles	C/G/T
Ancestral Allele	C
Minor Allele Frequence	0.0
Functional Annotation	missense_variant. Polyphen Annotation: benign(ENST00000374059, ENST00000362057' target='_blank'>ENST00000362057); probably damaging(ENST00000265134' target='_blank'>ENST00000265134, ENST00000362057' target='_blank'>ENST00000362057); possibly damaging(ENST00000265134' target='_blank'>ENST00000265134) SIFT Annotation: tolerated(ENST00000362057' target='_blank'>ENST00000362057, ENST00000374059' target='_blank'>ENST00000374059, ENST00000265134' target='_blank'>ENST00000265134); deleterious(ENST00000374059' target='_blank'>ENST00000374059, ENST00000265134' target='_blank'>ENST00000265134, ENST00000362057' target='_blank'>ENST00000362057)
Consequence to Transcript	missense_variant(ENST00000374059, ENST00000362057, ENST00000374059, ENST00000265134, ENST00000265134, ENST00000362057)
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
Takata, A.,2011(a)	C/G		Fisher's exact test: allele P-value = 1, genotype P-value = ...... Fisher's exact test: allele P-value = 1, genotype P-value = 1 More...	No significant association was observed in BD. No significant association was observed in BD.	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DFNB31	deafness, autosomal recessive 31	9q32	3(2/1/0)

SNPs in LD with rs35003670 (count: 0) View in gBrowse (chr9:114424482..114424482 )

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

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