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SNP Report
Name | rs17059506 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:28854394 - 28854394(1) | ||
Variant Alleles | G/A/C | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.229433 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000416984, ENST00000518510, ENST00000520184, ENST00000520437, ENST00000520831, ENST00000520983, ENST00000521022, ENST00000521777, ENST00000522363, ENST00000523303, ENST00000523436, ENST00000524081); NMD_transcript_variant(ENST00000518510, ENST00000520437, ENST00000522363, ENST00000523303); non_coding_transcript_variant(ENST00000520831, ENST00000520983) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |