SNP Report
Name | rs7718461 dbSNP Ensembl | ||
---|---|---|---|
Location | 5:76962223 - 76962223(+) | ||
Variant Seq | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.460463 | ||
Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000506501, ENST00000512446); upstream_gene_variant(ENST00000503763); intron_variant(ENST00000514258, ENST00000274368); non_coding_transcript_variant(ENST00000514258) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000274368) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000274368) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Genic enhancers;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |