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SNP Report
| Name | rs7118900 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr11:113396099 - 113396099(1) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.320487 | ||
| Functional Annotation | 3_prime_UTR_variant; missense_variant; NMD_transcript_variant.
Polyphen Annotation: benign(ENST00000303941) SIFT Annotation: tolerated(ENST00000303941) |
||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000542948); missense_variant(ENST00000303941); NMD_transcript_variant(ENST00000542948) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


