
Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
Name | rs1152230 dbSNP Ensembl | ||
---|---|---|---|
Location | chr19:49930246 - 49930246(1) | ||
Variant Alleles | G/A/C/T | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.291134 | ||
Functional Annotation | 5_prime_UTR_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000596658); intron_variant(ENST00000423777, ENST00000451973, ENST00000595125, ENST00000597227, ENST00000600336); NMD_transcript_variant(ENST00000451973); upstream_gene_variant(ENST00000341114, ENST00000352066, ENST00000422090, ENST00000578027, ENST00000593652, ENST00000594673, ENST00000595463, ENST00000595948, ENST00000596011, ENST00000596022, ENST00000596217, ENST00000596437, ENST00000596680, ENST00000597029, ENST00000597295, ENST00000597723, ENST00000597814, ENST00000598301, ENST00000599186, ENST00000599560, ENST00000599567, ENST00000599788, ENST00000599830, ENST00000600583, ENST00000600935, ENST00000601665, ENST00000601717) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |