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SNP Report
Name | rs3788358 dbSNP Ensembl | ||
---|---|---|---|
Location | chr22:23274168 - 23274168(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.324681 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000305877, ENST00000359540, ENST00000398512, ENST00000427791) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |