SNP Report
Name | rs58644381 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:149073231 - 149073231(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.21246 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000367463, ENST00000466695); non_coding_transcript_variant(ENST00000466695) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000367463) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000367463) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |