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SNP Report
Name | rs12539777 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:103420252 - 103420252(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.214058 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000306312, ENST00000339444, ENST00000354356, ENST00000356767, ENST00000393723, ENST00000393727, ENST00000393729, ENST00000393730, ENST00000393735, ENST00000423416, ENST00000432958, ENST00000445809, ENST00000454864, ENST00000456463, ENST00000487407); NMD_transcript_variant(ENST00000423416, ENST00000445809, ENST00000454864, ENST00000456463); non_coding_transcript_variant(ENST00000487407) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.