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SNP Report
Name | rs2585405 dbSNP Ensembl | ||
---|---|---|---|
Location | chr17:8143454 - 8143454(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.228235 | ||
Functional Annotation | downstream_gene_variant; intron_variant; missense_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000317276, ENST00000581082) SIFT Annotation: tolerated(ENST00000317276, ENST00000581082) |
||
Consequence to Transcript | downstream_gene_variant(ENST00000354903, ENST00000577424, ENST00000578223, ENST00000578950, ENST00000579203, ENST00000581395, ENST00000583559, ENST00000585095, ENST00000614952); intron_variant(ENST00000582719); missense_variant(ENST00000317276, ENST00000581082); NMD_transcript_variant(ENST00000582719); non_coding_transcript_exon_variant(ENST00000578089); non_coding_transcript_variant(ENST00000578089); upstream_gene_variant(ENST00000579098, ENST00000583677, ENST00000585284) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |