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SNP Report
Name | rs2989476 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:60593587 - 60593587(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.439497 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000439156, ENST00000634281, ENST00000634836, ENST00000635048, ENST00000635616); non_coding_transcript_variant(ENST00000439156, ENST00000634281, ENST00000634836, ENST00000635048, ENST00000635616) | ||
No. of Studies | 3 (Positive: 0; Negative: 2; 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.