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SNP Report
Name | rs16935888 dbSNP Ensembl | ||
---|---|---|---|
Location | chr10:35143477 - 35143477(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.159744 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000337656, ENST00000345491, ENST00000354759, ENST00000374721, ENST00000374726, ENST00000374728, ENST00000374734, ENST00000427847, ENST00000429130, ENST00000439705, ENST00000460270, ENST00000461968, ENST00000466251, ENST00000469949, ENST00000474362, ENST00000479070, ENST00000482633, ENST00000482646, ENST00000487132, ENST00000489321, ENST00000489388, ENST00000490460, ENST00000495960, ENST00000496019, ENST00000496626); NMD_transcript_variant(ENST00000490460, ENST00000495960); non_coding_transcript_variant(ENST00000461968, ENST00000466251, ENST00000482633, ENST00000482646, ENST00000489388, ENST00000496019, ENST00000496626); upstream_gene_variant(ENST00000348787, ENST00000464475) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | YES |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Crisafulli, C.,2012 | Association analysis:genotype P-value = >0.05;allele P-value > 0.05 | No significant association was observed in MDD. | Negative |