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SNP Report
Name | rs10082479 dbSNP Ensembl | ||
---|---|---|---|
Location | chr10:49621173 - 49621173(1) | ||
Variant Alleles | A/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.26877 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000481336, ENST00000490270); intron_variant(ENST00000337653, ENST00000339797, ENST00000351556, ENST00000395559, ENST00000395562, ENST00000460699, ENST00000466590); NMD_transcript_variant(ENST00000466590); non_coding_transcript_variant(ENST00000460699) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |