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SNP Report
Name | rs13139074 dbSNP Ensembl | ||
---|---|---|---|
Location | chr4:7480324 - 7480324(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.149161 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000329016, ENST00000507866, ENST00000511199); non_coding_transcript_variant(ENST00000511199) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; 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.