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- Data Summary
SNP Report
Basic Info
| Name | rs17574361 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr17:44108202(Fwd) | ||
| Variant Alleles | A/G/T/C | ||
| Ancestral Allele | A | ||
| Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000575318; ENST00000574590; ENST00000432791; ENST00000572904; ENST00000262419; ENST00000393476) downstream_gene_variant(ENST00000446361; ENST00000535772; ENST00000262410; ENST00000344290; ENST00000351559; ENST00000340799; ENST00000347967; ENST00000573682; ENST00000576137; ENST00000574963) nc_transcript_variant(ENST00000572218; ENST00000576870) non_coding_exon_variant(ENST00000572218; ENST00000576870) upstream_gene_variant(ENST00000570454) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 3)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 2)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.