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SNP Report
Name | rs9378490 dbSNP Ensembl | ||
---|---|---|---|
Location | chr6:7377362 - 7377362(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.372804 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000296742, ENST00000338150, ENST00000379918, ENST00000442019, ENST00000458291, ENST00000502583, ENST00000509324, ENST00000512086, ENST00000512691); NMD_transcript_variant(ENST00000442019, ENST00000458291); non_coding_transcript_variant(ENST00000509324) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |