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- Data Summary
SNP Report
Name | rs11881516 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr19:58757182(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000600029; ENST00000596677) intron_variant(ENST00000269829; ENST00000415203; ENST00000599227; ENST00000599953; ENST00000596677; ENST00000594384; ENST00000598880; ENST00000600044; ENST00000600775; ENST00000333581; ENST00000596652; ENST00000600029; ENST00000596929; ENST00000600220; ENST00000595981; ENST00000596825; ENST00000597240) nc_transcript_variant(ENST00000598880; ENST00000600775; ENST00000596597) non_coding_exon_variant(ENST00000596597) |
||
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.