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SNP Report
Name | rs1565922 dbSNP Ensembl | ||
---|---|---|---|
Location | chr17:39674782 - 39674782(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.444489 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000269582, ENST00000394246, ENST00000581428); intron_variant(ENST00000300658, ENST00000309862, ENST00000378011, ENST00000429199, ENST00000577337, ENST00000579146, ENST00000580898, ENST00000582276, ENST00000584620, ENST00000619169); NMD_transcript_variant(ENST00000577337, ENST00000584620); non_coding_transcript_variant(ENST00000309862, ENST00000580898, ENST00000582276) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |