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SNP Report
Name | rs9981892 dbSNP Ensembl | ||
---|---|---|---|
Location | chr21:46347094 - 46347094(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.161142 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000359568, ENST00000466474, ENST00000480896, ENST00000490468); non_coding_transcript_variant(ENST00000466474, ENST00000480896, ENST00000490468); upstream_gene_variant(ENST00000483844) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |