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SNP Report
Name | rs4953246 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:45752971 - 45752971(1) | ||
Variant Alleles | T/A/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.270367 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000306156, ENST00000421201, ENST00000467135, ENST00000476675, ENST00000480453, ENST00000485176, ENST00000497602); non_coding_transcript_variant(ENST00000467135, ENST00000476675, ENST00000480453, ENST00000485176, ENST00000497602) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |