SNP Report
Name | rs12373140 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:45846865 - 45846865(+) | ||
Variant Seq | A,C,T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.0860623 | ||
Annotation | synonymous_variant; missense_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | synonymous_variant(ENST00000329196); missense_variant(ENST00000329196); upstream_gene_variant(ENST00000581125); intron_variant(ENST00000579244, ENST00000634876, ENST00000579599); non_coding_transcript_variant(ENST00000579244, ENST00000634876, ENST00000579599) | ||
SIFT Annotation | tolerated_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000329196) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000329196) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |