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- Data Summary
SNP Report
Name | rs4568910 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr10:92662860(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000487998; ENST00000371703; ENST00000414836; ENST00000479678; ENST00000466462) intron_variant(ENST00000413330; ENST00000470933; ENST00000480406; ENST00000489806) nc_transcript_variant(ENST00000470933; ENST00000480406; ENST00000489806) |
||
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.