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SNP Report
| Name | rs6937334 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr6:17935773 - 17935773(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.283347 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000259711, ENST00000378814, ENST00000378826, ENST00000378843, ENST00000505588, ENST00000507576, ENST00000636847); non_coding_transcript_variant(ENST00000505588, ENST00000507576) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


