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SNP Report
Name | rs10516379 dbSNP Ensembl | ||
---|---|---|---|
Location | chr4:21299869 - 21299869(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.199481 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000382148, ENST00000382150, ENST00000382152, ENST00000447367, ENST00000509207, ENST00000515786); NMD_transcript_variant(ENST00000515786); upstream_gene_variant(ENST00000515680) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |