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SNP Report
Name | rs35776153 dbSNP Ensembl | ||
---|---|---|---|
Location | chr13:42189213 - 42189213(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele Frequence | 0.0 | ||
Functional Annotation | 3_prime_UTR_variant; missense_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Polyphen Annotation: benign(ENST00000261491, ENST00000337343, ENST00000379274, ENST00000536612, ENST00000627777, ENST00000628433) SIFT Annotation: tolerated(ENST00000261491, ENST00000337343, ENST00000379274, ENST00000536612, ENST00000627777, ENST00000628433) |
||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000626247); missense_variant(ENST00000261491, ENST00000337343, ENST00000379274, ENST00000536612, ENST00000627777, ENST00000628433); NMD_transcript_variant(ENST00000627777, ENST00000626247); non_coding_transcript_exon_variant(ENST00000498255); non_coding_transcript_variant(ENST00000498255) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |