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SNP Report
Name | rs4806874 dbSNP Ensembl | ||
---|---|---|---|
Location | chr19:2738354 - 2738354(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.460663 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000269740, ENST00000455372, ENST00000545664, ENST00000586572, ENST00000589166, ENST00000589363, ENST00000590875); non_coding_transcript_variant(ENST00000590875) | ||
No. of Studies | 2 (Positive: 0; Negative: 1; Trend: 1) | ||
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.