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- Data Summary
SNP Report
Name | rs1994798 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr1:11854755(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000376585; ENST00000376590; ENST00000376592; ENST00000376583) | ||
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.