SNP Report

Basic Info
Name |
rs72738786
dbSNP
Ensembl
|
Location |
15:78535744 - 78535744(+) |
Variant Seq |
T |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.177516 |
Annotation |
downstream_gene_variant; upstream_gene_variant; 3_prime_UTR_variant; intron_variant
|
Variant Effect |
downstream_gene_variant(ENST00000388988); upstream_gene_variant(ENST00000044462, ENST00000558635, ENST00000558639, ENST00000559948, ENST00000558281, ENST00000557929, ENST00000560033, ENST00000559146, ENST00000560099, ENST00000623556, ENST00000559365, ENST00000560217, ENST00000413382, ENST00000559082, ENST00000559934); 3_prime_UTR_variant(ENST00000569878); intron_variant(ENST00000563233, ENST00000408962)
|
SIFT Annotation |
tolerated
|
SIFT Variant Effect |
tolerated(ENST00000408962, ENST00000388988, ENST00000566332, ENST00000569878, ENST00000563233)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000408962, ENST00000388988, ENST00000566332, ENST00000569878, ENST00000563233)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
Chromatin interactive region
|
Chromatin State |
Weak transcription
|
No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
Source |
LD-proxy |

SNP related association results

SNP related genes (count: 2)

SNPs in LD with rs72738786 (count: 0)

SNP related eQTL (count: 1)