SNP Report

Basic Info
Name |
rs78826942
dbSNP
Ensembl
|
Location |
15:44103716 - 44103716(+) |
Variant Seq |
C |
Ancestral Allele |
T |
Ref Seq |
T |
Minor Allele Frequence |
0.01877 |
Annotation |
intron_variant; NMD_transcript_variant
|
Variant Effect |
intron_variant(ENST00000421674, ENST00000451277, ENST00000484674, ENST00000417257, ENST00000402883, ENST00000458630); NMD_transcript_variant(ENST00000421674, ENST00000451277, ENST00000458630)
|
SIFT Annotation |
deleterious
|
SIFT Variant Effect |
deleterious(ENST00000421674, ENST00000449926, ENST00000402883, ENST00000451277, ENST00000458630, ENST00000417257)
|
PolyPhen Annotation |
probably_damaging
|
PolyPhen Variant Effect |
probably_damaging(ENST00000421674, ENST00000449926, ENST00000402883, ENST00000451277, ENST00000458630, ENST00000417257)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;Bivalent Enhancer;Enhancers
|
No. of Marker's Association Results |
1 (Positive: 0; Negative: 0; Trend: 1) |
Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs78826942 (count: 0)

SNP related eQTL (count: 1)