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SNP Report
Name | rs1013442 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:27557399 - 27557399(1) | ||
Variant Alleles | A/T | ||
Ancestral Allele | A | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.180312 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000499008, ENST00000499568, ENST00000500662, ENST00000501176, ENST00000502161, ENST00000530686, ENST00000532965); non_coding_transcript_variant(ENST00000499008, ENST00000499568, ENST00000500662, ENST00000501176, ENST00000502161, ENST00000530686, ENST00000532965) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |