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SNP Report
Name | rs2282888 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:21436514 - 21436514(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.207268 | ||
Functional Annotation | intron_variant; NMD_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000222584, ENST00000432066, ENST00000448246); NMD_transcript_variant(ENST00000448246) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; 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.