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SNP Report
Name | rs1367959 dbSNP Ensembl | ||
---|---|---|---|
Location | chr15:26672011 - 26672011(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.246006 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000299267, ENST00000311550, ENST00000541819, ENST00000545868, ENST00000554556, ENST00000555094, ENST00000555632, ENST00000622697, ENST00000628124, ENST00000636466, ENST00000638099); NMD_transcript_variant(ENST00000554556, ENST00000555632); non_coding_transcript_variant(ENST00000555094) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |