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SNP Report
Name | rs3766507 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:147665106 - 147665106(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.211062 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000392988, ENST00000487562, ENST00000493129, ENST00000583509, ENST00000613673, ENST00000620634); NMD_transcript_variant(ENST00000620634); non_coding_transcript_variant(ENST00000613673) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |