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SNP Report
Name | rs1158827 dbSNP Ensembl | ||
---|---|---|---|
Location | chr20:10232894 - 10232894(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.121206 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000254976, ENST00000304886, ENST00000421143, ENST00000430336, ENST00000453544); non_coding_transcript_variant(ENST00000421143, ENST00000453544) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |