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- Data Summary
SNP Report
Name | rs13064466 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr3:113762574(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000460813; ENST00000463695) intron_variant(ENST00000472599; ENST00000480588; ENST00000545063; ENST00000460813; ENST00000491000; ENST00000483766; ENST00000463695; ENST00000295878; ENST00000481358) nc_transcript_variant(ENST00000480588; ENST00000481358) |
||
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.