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- Data Summary
SNP Report
Name | rs8071742 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:28361669(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000423598; ENST00000440741) intron_variant(ENST00000394835; ENST00000419434; ENST00000423598; ENST00000588978; ENST00000536908; ENST00000440741; ENST00000394832; ENST00000378738; ENST00000320856; ENST00000541045; ENST00000584826) nc_transcript_variant(ENST00000584826) |
||
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.