SNP Report

Basic Info
Name |
rs806376
dbSNP
Ensembl
|
Location |
6:88148929 - 88148929(+) |
Variant Seq |
C |
Ancestral Allele |
T |
Ref Seq |
T |
Minor Allele Frequence |
0.449681 |
Annotation |
upstream_gene_variant; intron_variant
|
Variant Effect |
upstream_gene_variant(ENST00000468898, ENST00000362094, ENST00000549890); intron_variant(ENST00000428600, ENST00000369499, ENST00000369501, ENST00000551417)
|
SIFT Annotation |
deleterious_-_low_confidence; tolerated_-_low_confidence; deleterious
|
SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000362094, ENST00000468898); tolerated_-_low_confidence(ENST00000549890, ENST00000369501, ENST00000428600, ENST00000369499); deleterious(ENST00000551417)
|
PolyPhen Annotation |
benign; probably_damaging
|
PolyPhen Variant Effect |
benign(ENST00000551417, ENST00000549890, ENST00000369501, ENST00000428600, ENST00000369499); probably_damaging(ENST00000362094, ENST00000468898)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak 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 rs806376 (count: 0)

SNP related eQTL (count: 1)