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SNP Report
Name | rs76869876 dbSNP Ensembl | ||
---|---|---|---|
Location | chr19:8949151 - 8949151(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.00579073 | ||
Functional Annotation | missense_variant.
Polyphen Annotation: unknown(ENST00000397910) |
||
Consequence to Transcript | missense_variant(ENST00000397910) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |