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SNP Report
Name | rs4398822 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:102926722 - 102926722(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.0551118 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000249377, ENST00000313221, ENST00000339431, ENST00000379305, ENST00000379308, ENST00000436908, ENST00000448002, ENST00000455112, ENST00000456695, ENST00000468216, ENST00000477915, ENST00000498487); NMD_transcript_variant(ENST00000448002); non_coding_transcript_variant(ENST00000468216, ENST00000477915, ENST00000498487) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |