SNP Report

Basic Info
Name |
rs38473
dbSNP
Ensembl
|
Location |
7:30553940 - 30553940(+) |
Variant Seq |
T |
Ancestral Allele |
T |
Ref Seq |
C |
Minor Allele Frequence |
0.204473 |
Annotation |
downstream_gene_variant; non_coding_transcript_exon_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000584621, ENST00000579437); non_coding_transcript_exon_variant(ENST00000355837); upstream_gene_variant(ENST00000582838, ENST00000625565, ENST00000440438, ENST00000598361); intron_variant(ENST00000577889, ENST00000631229, ENST00000434399, ENST00000626902, ENST00000578293, ENST00000426529, ENST00000578245, ENST00000580902, ENST00000578572); non_coding_transcript_variant(ENST00000577889, ENST00000631229, ENST00000434399, ENST00000626902, ENST00000578293, ENST00000355837, ENST00000426529, ENST00000578245, ENST00000580902, ENST00000578572)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000275428, ENST00000426081, ENST00000409436, ENST00000598361)
|
PolyPhen Annotation |
benign; probably_damaging
|
PolyPhen Variant Effect |
benign(ENST00000409436); probably_damaging(ENST00000275428, ENST00000426081, ENST00000598361)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
Chromatin interactive region;lncRNA
|
Chromatin State |
Weak transcription;Strong transcription;Enhancers
|
No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
Source |
LD-proxy |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs38473 (count: 0)

SNP related eQTL (count: 1)