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SNP Report
Name | rs11714419 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:52594800 - 52594800(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.308506 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000296302, ENST00000337303, ENST00000356770, ENST00000394830, ENST00000409057, ENST00000409114, ENST00000409767, ENST00000410007, ENST00000412587, ENST00000423351, ENST00000446103, ENST00000462207); NMD_transcript_variant(ENST00000412587); non_coding_transcript_variant(ENST00000462207) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |