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- Data Summary
SNP Report
Name | rs4472338 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr6:41664727(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000358871; ENST00000419788; ENST00000419574; ENST00000445214; ENST00000425401; ENST00000394283; ENST00000230323; ENST00000424495; ENST00000416140; ENST00000373033; ENST00000419396; ENST00000445700; ENST00000433032; ENST00000420312; ENST00000403298) | ||
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.