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- Data Summary
SNP Report
Name | rs174675 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr22:19934051(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000407537; ENST00000403184; ENST00000361682; ENST00000403710; ENST00000467943) nc_transcript_variant(ENST00000467943) upstream_gene_variant(ENST00000400525; ENST00000474308; ENST00000400519; ENST00000400521; ENST00000207636; ENST00000334363; ENST00000406520; ENST00000496729; ENST00000535882; ENST00000412786) |
||
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.