SNP Report

Basic Info
Name |
rs7503190
dbSNP
Ensembl
|
Location |
17:59106801 - 59106801(+) |
Variant Seq |
C |
Ancestral Allele |
C |
Ref Seq |
A |
Minor Allele Frequence |
0.388179 |
Annotation |
downstream_gene_variant; non_coding_transcript_exon_variant; 5_prime_UTR_variant; upstream_gene_variant; non_coding_transcript_variant
|
Variant Effect |
downstream_gene_variant(ENST00000330137); non_coding_transcript_exon_variant(ENST00000451775); 5_prime_UTR_variant(ENST00000393065, ENST00000393066); upstream_gene_variant(ENST00000625984, ENST00000577554, ENST00000584889, ENST00000580620, ENST00000580973, ENST00000580122, ENST00000583387, ENST00000262294); non_coding_transcript_variant(ENST00000451775)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000581068, ENST00000578105, ENST00000330137)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000581068, ENST00000578105, ENST00000330137)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
TF binding region;CpG island;Chromatin interactive region;lncRNA
|
Chromatin State |
Active TSS;Transcr. at gene 5' nd 3';Bivalent/Poised TSS
|
No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
Source |
LD-proxy |

SNP related association results

SNP related genes (count: 4)

SNPs in LD with rs7503190 (count: 0)

SNP related eQTL (count: 1)