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SNP Report
Name | rs10781084 dbSNP Ensembl | ||
---|---|---|---|
Location | chr9:72199542 - 72199542(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.30631 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000238018, ENST00000358399, ENST00000376986, ENST00000475764, ENST00000477618, ENST00000545168); NMD_transcript_variant(ENST00000475764); non_coding_transcript_variant(ENST00000477618) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |