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SNP Report
Name | rs4687638 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:52617950 - 52617950(1) | ||
Variant Alleles | A/C | ||
Ancestral Allele | A | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.314696 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000296302, ENST00000337303, ENST00000356770, ENST00000394830, ENST00000409057, ENST00000409114, ENST00000409767, ENST00000410007, ENST00000412587, ENST00000423351, ENST00000446103); NMD_transcript_variant(ENST00000412587); upstream_gene_variant(ENST00000480064) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |