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SNP Report
Name | rs11702278 dbSNP Ensembl | ||
---|---|---|---|
Location | chr21:46516382 - 46516382(1) | ||
Variant Alleles | T/G | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.429712 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000400274, ENST00000417564, ENST00000435722, ENST00000457905, ENST00000466639, ENST00000473752, ENST00000494435); non_coding_transcript_variant(ENST00000473752, ENST00000494435) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |