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- Data Summary
SNP Report
Name | rs30792 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:14386494(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000512070) intron_variant(ENST00000344204; ENST00000537187; ENST00000509967; ENST00000515144; ENST00000512070; ENST00000513206) nc_transcript_variant(ENST00000515144) upstream_gene_variant(ENST00000510757; ENST00000502490) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.