SNP Report
Name | rs2073836 dbSNP Ensembl | ||
---|---|---|---|
Location | 9:133667012 - 133667012(+) | ||
Variant Seq | T | ||
Ancestral Allele | T | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.368411 | ||
Annotation | non_coding_transcript_exon_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | non_coding_transcript_exon_variant(ENST00000469828); intron_variant(ENST00000371872, ENST00000439388, ENST00000371868, ENST00000422262); non_coding_transcript_variant(ENST00000469828) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000393056) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000393056) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | lncRNA | ||
Chromatin State | Weak transcription;Genic enhancers;Enhancers;Strong transcription;Bivalent Enhancer | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |