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SNP Report
Name | rs579528 dbSNP Ensembl | ||
---|---|---|---|
Location | chr6:118599826 - 118599826(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.0385383 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000360290, ENST00000368488, ENST00000368491, ENST00000392500, ENST00000419517, ENST00000434604, ENST00000462101, ENST00000476150, ENST00000483035); non_coding_transcript_variant(ENST00000462101, ENST00000476150, ENST00000483035) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |