SNP Report

Basic Info
Name |
rs58428316
dbSNP
Ensembl
|
Location |
6:15648444 - 15648444(+) |
Variant Seq |
A |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.104633 |
Annotation |
intron_variant; NMD_transcript_variant
|
Variant Effect |
intron_variant(ENST00000355917, ENST00000622898, ENST00000515875, ENST00000338950, ENST00000510395, ENST00000506844, LRG_588t2, ENST00000344537, ENST00000513680, LRG_588t1, ENST00000511762); NMD_transcript_variant(ENST00000515875, ENST00000510395, ENST00000506844, ENST00000513680)
|
SIFT Annotation |
deleterious_-_low_confidence; deleterious
|
SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000510395); deleterious(ENST00000515875, ENST00000344537, ENST00000355917, LRG_588t2, ENST00000338950, LRG_588t1)
|
PolyPhen Annotation |
probably_damaging
|
PolyPhen Variant Effect |
probably_damaging(ENST00000515875, ENST00000510395, ENST00000344537, ENST00000355917, LRG_588t2, ENST00000338950, LRG_588t1)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;ZNF genes & repeats;Strong 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 rs58428316 (count: 0)

SNP related eQTL (count: 1)