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SNP Report
Name | rs7581712 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:160144658 - 160144658(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.213858 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000283249, ENST00000409583, ENST00000409872, ENST00000409967, ENST00000428609, ENST00000485635, ENST00000620391); NMD_transcript_variant(ENST00000409583); non_coding_transcript_variant(ENST00000485635) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |