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SNP Report
Name | rs13005832 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:154376679 - 154376679(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.111621 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000392825, ENST00000409237, ENST00000431076, ENST00000450838, ENST00000487047); NMD_transcript_variant(ENST00000431076); non_coding_transcript_variant(ENST00000487047) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |