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SNP Report
Name | rs12489404 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:7305011 - 7305011(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.42492 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000357716, ENST00000389335, ENST00000389336, ENST00000402647, ENST00000435689, ENST00000440923, ENST00000448328, ENST00000461677, ENST00000463676, ENST00000467425, ENST00000486284); NMD_transcript_variant(ENST00000389335, ENST00000435689, ENST00000440923, ENST00000467425); non_coding_transcript_variant(ENST00000461677, ENST00000463676) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |