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SNP Report
Name | rs4822697 dbSNP Ensembl | ||
---|---|---|---|
Location | chr22:26245269 - 26245269(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.246406 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000248933, ENST00000343706, ENST00000360929, ENST00000404234, ENST00000414989, ENST00000529632, ENST00000629590); non_coding_transcript_variant(ENST00000414989) | ||
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.