SNP Report

Basic Info
Name |
rs11978620
dbSNP
Ensembl
|
Location |
7:31090247 - 31090247(+) |
Variant Seq |
T |
Ancestral Allele |
T |
Ref Seq |
C |
Minor Allele Frequence |
0.115815 |
Annotation |
intron_variant
|
Variant Effect |
intron_variant(ENST00000409363, ENST00000436116, ENST00000614107, ENST00000409489, ENST00000304166, ENST00000396211)
|
SIFT Annotation |
deleterious; tolerated
|
SIFT Variant Effect |
deleterious(ENST00000614107, ENST00000409489, ENST00000396211); tolerated(ENST00000409363, ENST00000304166)
|
PolyPhen Annotation |
benign
|
PolyPhen Variant Effect |
benign(ENST00000614107, ENST00000409363, ENST00000304166, ENST00000409489, ENST00000396211)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
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: 1)

SNPs in LD with rs11978620 (count: 0)

SNP related eQTL (count: 1)