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SNP Report
Name | rs28505970 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:1173095 - 1173095(1) | ||
Variant Alleles | C/A | ||
Ancestral Allele | C | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.20627 | ||
Functional Annotation | intron_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Polyphen Annotation: probably damaging(ENST00000308624) SIFT Annotation: deleterious(ENST00000308624) |
||
Consequence to Transcript | intron_variant(ENST00000407292); missense_variant(ENST00000308624); non_coding_transcript_exon_variant(ENST00000463442, ENST00000467759, ENST00000475201, ENST00000494178); non_coding_transcript_variant(ENST00000463442, ENST00000467759, ENST00000475201, ENST00000494178) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |