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SNP Report
Name | rs2241165 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:170821869 - 170821869(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.381789 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000344257, ENST00000358196, ENST00000375272, ENST00000414527, ENST00000429023, ENST00000445006, ENST00000454603, ENST00000455008, ENST00000456864, ENST00000493875, ENST00000625689); NMD_transcript_variant(ENST00000414527, ENST00000493875); non_coding_transcript_exon_variant(ENST00000485013); non_coding_transcript_variant(ENST00000429023, ENST00000485013); upstream_gene_variant(ENST00000418106, ENST00000451730, ENST00000455988, ENST00000486850) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.