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- Data Summary
SNP Report
Name | rs7099565 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr10:116719543(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Functional Annotation | missense_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | missense_variant(ENST00000298746) nc_transcript_variant(ENST00000485065) non_coding_exon_variant(ENST00000485065) |
||
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.