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SNP Report
Name | rs13322211 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:77176746 - 77176746(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.330471 | ||
Functional Annotation | intron_variant; NMD_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000332191, ENST00000461745, ENST00000473767, ENST00000487694, ENST00000602589); NMD_transcript_variant(ENST00000473767) | ||
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.