SNP Report
Name | rs1799983 dbSNP Ensembl |
---|---|
Location | Chrchr7:150696111(Forward) |
Variant Alleles | T/G |
Ancestral Allele | |
Annotation |
intron_variant; missense_variant; upstream_gene_variant
PolyPhen: benign(ENST00000297494, ENST00000461406, ENST00000467517, ENST00000484524) SIFT: tolerated(ENST00000297494, ENST00000461406, ENST00000467517, ENST00000484524) |
Consequence to Transcript | intron_variant(ENST00000484576) missense_variant(ENST00000297494, ENST00000461406, ENST00000467517, ENST00000484524) upstream_gene_variant(ENST00000460603) |
No. of Studies (Positive/Negative) | 1 (0/1) |