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SNP Report
Name | rs35003670 dbSNP Ensembl | ||
---|---|---|---|
Location | chr9:114424482 - 114424482(1) | ||
Variant Alleles | C/G/T | ||
Ancestral Allele | C | ||
Minor Allele Frequence | 0.0 | ||
Functional Annotation | missense_variant.
Polyphen Annotation: benign(ENST00000374059, ENST00000362057' target='_blank'>ENST00000362057); probably damaging(ENST00000265134' target='_blank'>ENST00000265134, ENST00000362057' target='_blank'>ENST00000362057); possibly damaging(ENST00000265134' target='_blank'>ENST00000265134) SIFT Annotation: tolerated(ENST00000362057' target='_blank'>ENST00000362057, ENST00000374059' target='_blank'>ENST00000374059, ENST00000265134' target='_blank'>ENST00000265134); deleterious(ENST00000374059' target='_blank'>ENST00000374059, ENST00000265134' target='_blank'>ENST00000265134, ENST00000362057' target='_blank'>ENST00000362057) |
||
Consequence to Transcript | missense_variant(ENST00000374059, ENST00000362057, ENST00000374059, ENST00000265134, ENST00000265134, ENST00000362057) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |