SNP Report
Name | rs9688674 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:35510027 - 35510027(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.0453275 | ||
Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000448446); upstream_gene_variant(ENST00000496434); intron_variant(ENST00000373892, ENST00000428978, ENST00000322263, ENST00000614066, ENST00000229771); non_coding_transcript_variant(ENST00000373892) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000229771, ENST00000614066); tolerated(ENST00000322263) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000229771, ENST00000614066, ENST00000322263) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Enhancers;Bivalent Enhancer | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |