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SNP Report
Name | rs17646069 dbSNP Ensembl | ||
---|---|---|---|
Location | chr13:42229127 - 42229127(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.0623003 | ||
Functional Annotation | 3_prime_UTR_variant; missense_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
Polyphen Annotation: benign(ENST00000536612, ENST00000628433, ENST00000337343) SIFT Annotation: tolerated(ENST00000337343); deleterious(ENST00000536612, ENST00000628433) |
||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000626247, ENST00000627777); missense_variant(ENST00000536612, ENST00000628433, ENST00000337343); NMD_transcript_variant(ENST00000626247, ENST00000627777); non_coding_transcript_exon_variant(ENST00000498255); non_coding_transcript_variant(ENST00000498255); synonymous_variant(ENST00000261491, ENST00000379274) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |