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SNP Report
Name | rs555446 dbSNP Ensembl | ||
---|---|---|---|
Location | chr18:10545921 - 10545921(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.423123 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000322897, ENST00000580224, ENST00000580483, ENST00000583367); NMD_transcript_variant(ENST00000580224, ENST00000580483); non_coding_transcript_variant(ENST00000583367) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |